Canonical Allele Identifier: CA2580068759

Gene: ATP2C1

Linked Data

• ClinVar Variation Id: 2031331
• ClinVar RCV Id: RCV002867129

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.130997618_130997621del , CM000665.2:g.130997618_130997621del	GRCh38
NC_000003.11:g.130716462_130716465del , CM000665.1:g.130716462_130716465del	GRCh37
NC_000003.10:g.132199152_132199155del	NCBI36
NG_007379.1:g.108029_108032del
NG_007379.2:g.152094_152097del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510168.6:c.2256_2259del MANE Select	ENSP00000427461.1:p.Pro753TrpfsTer18
ENST00000328560.12:c.2256_2259del	ENSP00000329664.8:p.Pro753TrpfsTer18
ENST00000359644.7:c.2256_2259del	ENSP00000352665.3:p.Pro753TrpfsTer18
ENST00000422190.6:c.2256_2259del	ENSP00000402677.2:p.Pro753TrpfsTer18
ENST00000428331.6:c.2256_2259del	ENSP00000395809.2:p.Pro753TrpfsTer18
ENST00000504381.5:c.2241_2244del	ENSP00000425320.2:p.Pro748TrpfsTer18
ENST00000504612.5:c.2117_2120del
ENST00000504948.5:c.2208_2211del	ENSP00000423330.1:p.Pro737TrpfsTer18
ENST00000505330.5:c.2358_2361del	ENSP00000423774.2:p.Pro787TrpfsTer18
ENST00000507194.1:c.155_158del	ENSP00000427087.1:n.155_158del
ENST00000507488.6:c.2358_2361del	ENSP00000421326.3:p.Pro787TrpfsTer18
ENST00000508532.5:c.2256_2259del	ENSP00000424783.1:p.Pro753TrpfsTer18
ENST00000508660.5:c.809_812del
ENST00000510168.5:c.2256_2259del	ENSP00000427461.1:p.Pro753TrpfsTer18
ENST00000513801.5:c.2208_2211del	ENSP00000422872.1:p.Pro737TrpfsTer18
ENST00000514654.5:n.2426_2429del
ENST00000533801.6:c.2256_2259del	ENSP00000432956.3:p.Pro753TrpfsTer18
NM_001001485.2:c.2256_2259del	NP_001001485.1:p.Pro753TrpfsTer18
NM_001001486.1:c.2256_2259del	NP_001001486.1:p.Pro753TrpfsTer18
NM_001001487.1:c.2256_2259del	NP_001001487.1:p.Pro753TrpfsTer18
NM_001199179.1:c.2256_2259del	NP_001186108.1:p.Pro753TrpfsTer18
NM_001199180.1:c.2358_2361del	NP_001186109.1:p.Pro787TrpfsTer18
NM_001199181.1:c.2358_2361del	NP_001186110.1:p.Pro787TrpfsTer18
NM_001199182.1:c.2241_2244del	NP_001186111.1:p.Pro748TrpfsTer18
NM_001199183.1:c.2208_2211del	NP_001186112.1:p.Pro737TrpfsTer18
NM_001199184.1:c.2208_2211del	NP_001186113.1:p.Pro737TrpfsTer18
NM_001199185.1:c.2256_2259del	NP_001186114.1:p.Pro753TrpfsTer18
NM_014382.3:c.2256_2259del	NP_055197.2:p.Pro753TrpfsTer18
XM_005247354.1:c.2358_2361del	XP_005247411.1:p.Pro787TrpfsTer18
XM_005247355.1:c.2256_2259del	XP_005247412.1:p.Pro753TrpfsTer18
XM_005247356.1:c.2256_2259del	XP_005247413.1:p.Pro753TrpfsTer18
XM_005247357.1:c.2256_2259del	XP_005247414.1:p.Pro753TrpfsTer18
XM_005247358.1:c.2208_2211del	XP_005247415.1:p.Pro737TrpfsTer18
XM_006713585.1:c.2256_2259del	XP_006713648.1:p.Pro753TrpfsTer18
XM_011512685.1:c.2187_2190del	XP_011510987.1:p.Pro730TrpfsTer18
XM_011512686.1:c.1422_1425del	XP_011510988.1:p.Pro475TrpfsTer18
XM_005247354.2:c.2358_2361del	XP_005247411.1:p.Pro787TrpfsTer18
XM_005247355.2:c.2256_2259del	XP_005247412.1:p.Pro753TrpfsTer18
XM_005247356.3:c.2256_2259del	XP_005247413.1:p.Pro753TrpfsTer18
XM_005247358.3:c.2208_2211del	XP_005247415.1:p.Pro737TrpfsTer18
XM_011512686.2:c.1422_1425del	XP_011510988.1:p.Pro475TrpfsTer18
XM_017006164.2:c.2256_2259del	XP_016861653.1:p.Pro753TrpfsTer18
NM_001199179.2:c.2256_2259del	NP_001186108.1:p.Pro753TrpfsTer18
NM_001199180.2:c.2358_2361del	NP_001186109.1:p.Pro787TrpfsTer18
NM_001199181.2:c.2358_2361del	NP_001186110.1:p.Pro787TrpfsTer18
NM_001199182.2:c.2241_2244del	NP_001186111.1:p.Pro748TrpfsTer18
NM_001199183.2:c.2208_2211del	NP_001186112.1:p.Pro737TrpfsTer18
NM_001199184.2:c.2208_2211del	NP_001186113.1:p.Pro737TrpfsTer18
NM_001199185.2:c.2256_2259del	NP_001186114.1:p.Pro753TrpfsTer18
NM_014382.4:c.2256_2259del	NP_055197.2:p.Pro753TrpfsTer18
NM_001001485.3:c.2256_2259del	NP_001001485.1:p.Pro753TrpfsTer18
NM_001001486.2:c.2256_2259del	NP_001001486.1:p.Pro753TrpfsTer18
NM_001001487.2:c.2256_2259del	NP_001001487.1:p.Pro753TrpfsTer18
NM_001199179.3:c.2256_2259del	NP_001186108.1:p.Pro753TrpfsTer18
NM_001199181.3:c.2358_2361del	NP_001186110.1:p.Pro787TrpfsTer18
NM_001199184.3:c.2208_2211del	NP_001186113.1:p.Pro737TrpfsTer18
NM_001378511.1:c.2358_2361del	NP_001365440.1:p.Pro787TrpfsTer18
NM_001378512.1:c.2256_2259del	NP_001365441.1:p.Pro753TrpfsTer18
NM_001378513.1:c.2256_2259del	NP_001365442.1:p.Pro753TrpfsTer18
NM_001378514.1:c.2208_2211del	NP_001365443.1:p.Pro737TrpfsTer18
NM_001378687.1:c.2256_2259del MANE Select	NP_001365616.1:p.Pro753TrpfsTer18
NM_014382.5:c.2256_2259del	NP_055197.2:p.Pro753TrpfsTer18