Canonical Allele Identifier: CA348406604

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186431A>C (hg19) ; chr2:g.127428855A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428855A>C , CM000664.2:g.127428855A>C	GRCh38
NC_000002.11:g.128186431A>C , CM000664.1:g.128186431A>C	GRCh37
NC_000002.10:g.127902901A>C	NCBI36
NG_016323.1:g.15436A>C , LRG_599:g.15436A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1295A>C MANE Select	ENSP00000234071.4:p.Tyr432Ser
ENST00000234071.7:c.1295A>C	ENSP00000234071.3:p.Tyr432Ser
ENST00000402125.2:c.619A>C
ENST00000409048.1:c.1397A>C	ENSP00000386679.1:p.Tyr466Ser
NM_000312.3:c.1295A>C , LRG_599t1:c.1295A>C	NP_000303.1:p.Tyr432Ser
XM_005263715.3:c.1478A>C	XP_005263772.1:p.Tyr493Ser
XM_005263716.3:c.1460A>C	XP_005263773.1:p.Tyr487Ser
XM_005263717.3:c.1358A>C	XP_005263774.1:p.Tyr453Ser
XR_923313.1:n.1332-591T>G
XM_005263717.4:c.1358A>C	XP_005263774.1:p.Tyr453Ser
XM_017004505.1:c.1538A>C	XP_016859994.1:p.Tyr513Ser
XM_024453002.1:c.1640A>C	XP_024308770.1:p.Tyr547Ser
XM_024453003.1:c.1580A>C	XP_024308771.1:p.Tyr527Ser
XM_024453004.1:c.1478A>C	XP_024308772.1:p.Tyr493Ser
XM_024453005.1:c.1460A>C	XP_024308773.1:p.Tyr487Ser
XM_024453006.1:c.1397A>C	XP_024308774.1:p.Tyr466Ser
XR_001739705.1:n.3607-591T>G
XR_923313.2:n.4043-591T>G
NM_000312.4:c.1295A>C MANE Select	NP_000303.1:p.Tyr432Ser
NM_001375602.1:c.1478A>C	NP_001362531.1:p.Tyr493Ser
NM_001375603.1:c.1460A>C	NP_001362532.1:p.Tyr487Ser
NM_001375604.1:c.1358A>C	NP_001362533.1:p.Tyr453Ser
NM_001375605.1:c.1397A>C	NP_001362534.1:p.Tyr466Ser
NM_001375606.1:c.1463A>C	NP_001362535.1:p.Tyr488Ser
NM_001375607.1:c.1481A>C	NP_001362536.1:p.Tyr494Ser
NM_001375608.1:c.1238A>C	NP_001362537.1:p.Tyr413Ser
NM_001375609.1:c.1271A>C	NP_001362538.1:p.Tyr424Ser
NM_001375610.1:c.1289A>C	NP_001362539.1:p.Tyr430Ser
NM_001375611.1:c.1295A>C	NP_001362540.1:p.Tyr432Ser
NM_001375613.1:c.1295A>C	NP_001362542.1:p.Tyr432Ser