Canonical Allele Identifier: CA1401886981

Gene: ATP2C1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.130980431T= , CM000665.2:g.130980431T=	GRCh38
NC_000003.11:g.130699275T= , CM000665.1:g.130699275T=	GRCh37
NC_000003.10:g.132181965T=	NCBI36
NG_007379.1:g.90842T=
NG_007379.2:g.134907T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510168.6:c.1742-151T= MANE Select	ENSP00000427461.1:n.1742-151T=
ENST00000328560.12:c.1742-151T=	ENSP00000329664.8:n.1742-151T=
ENST00000359644.7:c.1742-151T=	ENSP00000352665.3:n.1742-151T=
ENST00000422190.6:c.1742-151T=	ENSP00000402677.2:n.1742-151T=
ENST00000428331.6:c.1742-151T=	ENSP00000395809.2:n.1742-151T=
ENST00000504381.5:c.1727-151T=	ENSP00000425320.2:n.1727-151T=
ENST00000504571.5:c.631+4943T=	ENSP00000422489.1:n.631+4943T=
ENST00000504612.5:c.1603-151T=
ENST00000504948.5:c.1694-151T=	ENSP00000423330.1:n.1694-151T=
ENST00000505330.5:c.1844-151T=	ENSP00000423774.2:n.1844-151T=
ENST00000507488.6:c.1844-151T=	ENSP00000421326.3:n.1844-151T=
ENST00000508532.5:c.1742-151T=	ENSP00000424783.1:n.1742-151T=
ENST00000508660.5:c.295-151T=
ENST00000510168.5:c.1742-151T=	ENSP00000427461.1:n.1742-151T=
ENST00000513801.5:c.1694-151T=	ENSP00000422872.1:n.1694-151T=
ENST00000514654.5:n.1912-151T=
ENST00000533801.6:c.1742-151T=	ENSP00000432956.3:n.1742-151T=
NM_001001485.2:c.1742-151T=	NP_001001485.1:n.1742-151T=
NM_001001486.1:c.1742-151T=	NP_001001486.1:n.1742-151T=
NM_001001487.1:c.1742-151T=	NP_001001487.1:n.1742-151T=
NM_001199179.1:c.1742-151T=	NP_001186108.1:n.1742-151T=
NM_001199180.1:c.1844-151T=	NP_001186109.1:n.1844-151T=
NM_001199181.1:c.1844-151T=	NP_001186110.1:n.1844-151T=
NM_001199182.1:c.1727-151T=	NP_001186111.1:n.1727-151T=
NM_001199183.1:c.1694-151T=	NP_001186112.1:n.1694-151T=
NM_001199184.1:c.1694-151T=	NP_001186113.1:n.1694-151T=
NM_001199185.1:c.1742-151T=	NP_001186114.1:n.1742-151T=
NM_014382.3:c.1742-151T=	NP_055197.2:n.1742-151T=
XM_005247354.1:c.1844-151T=	XP_005247411.1:n.1844-151T=
XM_005247355.1:c.1742-151T=	XP_005247412.1:n.1742-151T=
XM_005247356.1:c.1742-151T=	XP_005247413.1:n.1742-151T=
XM_005247357.1:c.1742-151T=	XP_005247414.1:n.1742-151T=
XM_005247358.1:c.1694-151T=	XP_005247415.1:n.1694-151T=
XM_006713585.1:c.1742-151T=	XP_006713648.1:n.1742-151T=
XM_011512685.1:c.1673-151T=	XP_011510987.1:n.1673-151T=
XM_011512686.1:c.908-151T=	XP_011510988.1:n.908-151T=
XM_011512687.1:c.1672+4943T=	XP_011510989.1:n.1672+4943T=
XM_005247354.2:c.1844-151T=	XP_005247411.1:n.1844-151T=
XM_005247355.2:c.1742-151T=	XP_005247412.1:n.1742-151T=
XM_005247356.3:c.1742-151T=	XP_005247413.1:n.1742-151T=
XM_005247358.3:c.1694-151T=	XP_005247415.1:n.1694-151T=
XM_011512686.2:c.908-151T=	XP_011510988.1:n.908-151T=
XM_017006164.2:c.1742-151T=	XP_016861653.1:n.1742-151T=
NM_001199179.2:c.1742-151T=	NP_001186108.1:n.1742-151T=
NM_001199180.2:c.1844-151T=	NP_001186109.1:n.1844-151T=
NM_001199181.2:c.1844-151T=	NP_001186110.1:n.1844-151T=
NM_001199182.2:c.1727-151T=	NP_001186111.1:n.1727-151T=
NM_001199183.2:c.1694-151T=	NP_001186112.1:n.1694-151T=
NM_001199184.2:c.1694-151T=	NP_001186113.1:n.1694-151T=
NM_001199185.2:c.1742-151T=	NP_001186114.1:n.1742-151T=
NM_014382.4:c.1742-151T=	NP_055197.2:n.1742-151T=
NM_001001485.3:c.1742-151T=	NP_001001485.1:n.1742-151T=
NM_001001486.2:c.1742-151T=	NP_001001486.1:n.1742-151T=
NM_001001487.2:c.1742-151T=	NP_001001487.1:n.1742-151T=
NM_001199179.3:c.1742-151T=	NP_001186108.1:n.1742-151T=
NM_001199181.3:c.1844-151T=	NP_001186110.1:n.1844-151T=
NM_001199184.3:c.1694-151T=	NP_001186113.1:n.1694-151T=
NM_001378511.1:c.1844-151T=	NP_001365440.1:n.1844-151T=
NM_001378512.1:c.1742-151T=	NP_001365441.1:n.1742-151T=
NM_001378513.1:c.1742-151T=	NP_001365442.1:n.1742-151T=
NM_001378514.1:c.1694-151T=	NP_001365443.1:n.1694-151T=
NM_001378687.1:c.1742-151T= MANE Select	NP_001365616.1:n.1742-151T=
NM_014382.5:c.1742-151T=	NP_055197.2:n.1742-151T=