Canonical Allele Identifier: CA348405332

Gene: PROC

Linked Data

• dbSNP Id: rs121918150
• MyVariant Identifiers: chr2:g.128186136G>C (hg19) ; chr2:g.127428560G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428560G>C , CM000664.2:g.127428560G>C	GRCh38
NC_000002.11:g.128186136G>C , CM000664.1:g.128186136G>C	GRCh37
NC_000002.10:g.127902606G>C	NCBI36
NG_016323.1:g.15141G>C , LRG_599:g.15141G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1000G>C MANE Select	ENSP00000234071.4:p.Gly334Arg
ENST00000234071.7:c.1000G>C	ENSP00000234071.3:p.Gly334Arg
ENST00000402125.2:c.324G>C
ENST00000409048.1:c.1102G>C	ENSP00000386679.1:p.Gly368Arg
NM_000312.3:c.1000G>C , LRG_599t1:c.1000G>C	NP_000303.1:p.Gly334Arg
XM_005263715.3:c.1183G>C	XP_005263772.1:p.Gly395Arg
XM_005263716.3:c.1165G>C	XP_005263773.1:p.Gly389Arg
XM_005263717.3:c.1063G>C	XP_005263774.1:p.Gly355Arg
XR_923313.1:n.1332-296C>G
XM_005263717.4:c.1063G>C	XP_005263774.1:p.Gly355Arg
XM_017004505.1:c.1243G>C	XP_016859994.1:p.Gly415Arg
XM_024453002.1:c.1345G>C	XP_024308770.1:p.Gly449Arg
XM_024453003.1:c.1285G>C	XP_024308771.1:p.Gly429Arg
XM_024453004.1:c.1183G>C	XP_024308772.1:p.Gly395Arg
XM_024453005.1:c.1165G>C	XP_024308773.1:p.Gly389Arg
XM_024453006.1:c.1102G>C	XP_024308774.1:p.Gly368Arg
XR_001739705.1:n.3607-296C>G
XR_923313.2:n.4043-296C>G
NM_000312.4:c.1000G>C MANE Select	NP_000303.1:p.Gly334Arg
NM_001375602.1:c.1183G>C	NP_001362531.1:p.Gly395Arg
NM_001375603.1:c.1165G>C	NP_001362532.1:p.Gly389Arg
NM_001375604.1:c.1063G>C	NP_001362533.1:p.Gly355Arg
NM_001375605.1:c.1102G>C	NP_001362534.1:p.Gly368Arg
NM_001375606.1:c.1168G>C	NP_001362535.1:p.Gly390Arg
NM_001375607.1:c.1186G>C	NP_001362536.1:p.Gly396Arg
NM_001375608.1:c.943G>C	NP_001362537.1:p.Gly315Arg
NM_001375609.1:c.976G>C	NP_001362538.1:p.Gly326Arg
NM_001375610.1:c.994G>C	NP_001362539.1:p.Gly332Arg
NM_001375611.1:c.1000G>C	NP_001362540.1:p.Gly334Arg
NM_001375613.1:c.1000G>C	NP_001362542.1:p.Gly334Arg