Canonical Allele Identifier: CA2582341509

Gene: APC

Linked Data

• ClinVar Variation Id: 2583998
• ClinVar RCV Id: RCV003334920 ; RCV003535009

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838922del , CM000667.2:g.112838922del	GRCh38
NC_000005.9:g.112174619del , CM000667.1:g.112174619del	GRCh37
NC_000005.8:g.112202518del	NCBI36
NG_008481.4:g.151402del , LRG_130:g.151402del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2993del	ENSP00000484935.2:n.2993del
ENST00000504915.3:c.3382del	ENSP00000473355.2:p.Ser1128GlnfsTer16
ENST00000505350.2:c.*3334del	ENSP00000481752.1:n.*3334del
ENST00000507379.6:c.3274del	ENSP00000423224.2:p.Ser1092GlnfsTer16
ENST00000509732.6:c.3328del	ENSP00000426541.2:p.Ser1110GlnfsTer16
ENST00000512211.7:c.3328del	ENSP00000423828.3:p.Ser1110GlnfsTer16
ENST00000257430.9:c.3328del MANE Select	ENSP00000257430.4:p.Ser1110GlnfsTer16
ENST00000257430.8:c.3328del	ENSP00000257430.4:p.Ser1110GlnfsTer16
ENST00000502371.2:c.1681del
ENST00000507379.5:c.3274del	ENSP00000423224.1:p.Ser1092GlnfsTer16
ENST00000508376.6:c.3328del	ENSP00000427089.2:p.Ser1110GlnfsTer16
ENST00000508624.5:c.*2650del	ENSP00000424265.1:n.*2650del
ENST00000512211.6:c.3328del	ENSP00000423828.2:p.Ser1110GlnfsTer16
ENST00000520401.1:c.230+9950del
NM_000038.5:c.3328del	NP_000029.2:p.Ser1110GlnfsTer16
NM_001127510.2:c.3328del	NP_001120982.1:p.Ser1110GlnfsTer16
NM_001127511.2:c.3274del	NP_001120983.2:p.Ser1092GlnfsTer16
NM_001354895.1:c.3328del	NP_001341824.1:p.Ser1110GlnfsTer16
NM_001354896.1:c.3382del	NP_001341825.1:p.Ser1128GlnfsTer16
NM_001354897.1:c.3358del	NP_001341826.1:p.Ser1120GlnfsTer16
NM_001354898.1:c.3253del	NP_001341827.1:p.Ser1085GlnfsTer16
NM_001354899.1:c.3244del	NP_001341828.1:p.Ser1082GlnfsTer16
NM_001354900.1:c.3205del	NP_001341829.1:p.Ser1069GlnfsTer16
NM_001354901.1:c.3151del	NP_001341830.1:p.Ser1051GlnfsTer16
NM_001354902.1:c.3055del	NP_001341831.1:p.Ser1019GlnfsTer16
NM_001354903.1:c.3025del	NP_001341832.1:p.Ser1009GlnfsTer16
NM_001354904.1:c.2950del	NP_001341833.1:p.Ser984GlnfsTer16
NM_001354905.1:c.2848del	NP_001341834.1:p.Ser950GlnfsTer16
NM_001354906.1:c.2479del	NP_001341835.1:p.Ser827GlnfsTer16
NM_000038.6:c.3328del MANE Select	NP_000029.2:p.Ser1110GlnfsTer16
NM_001127510.3:c.3328del	NP_001120982.1:p.Ser1110GlnfsTer16
NM_001127511.3:c.3274del	NP_001120983.2:p.Ser1092GlnfsTer16
NM_001354895.2:c.3328del	NP_001341824.1:p.Ser1110GlnfsTer16
NM_001354896.2:c.3382del	NP_001341825.1:p.Ser1128GlnfsTer16
NM_001354897.2:c.3358del	NP_001341826.1:p.Ser1120GlnfsTer16
NM_001354898.2:c.3253del	NP_001341827.1:p.Ser1085GlnfsTer16
NM_001354899.2:c.3244del	NP_001341828.1:p.Ser1082GlnfsTer16
NM_001354900.2:c.3205del	NP_001341829.1:p.Ser1069GlnfsTer16
NM_001354901.2:c.3151del	NP_001341830.1:p.Ser1051GlnfsTer16
NM_001354902.2:c.3055del	NP_001341831.1:p.Ser1019GlnfsTer16
NM_001354903.2:c.3025del	NP_001341832.1:p.Ser1009GlnfsTer16
NM_001354904.2:c.2950del	NP_001341833.1:p.Ser984GlnfsTer16
NM_001354905.2:c.2848del	NP_001341834.1:p.Ser950GlnfsTer16
NM_001354906.2:c.2479del	NP_001341835.1:p.Ser827GlnfsTer16