Canonical Allele Identifier: CA428871821

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186129T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428553T>C , CM000664.2:g.127428553T>C	GRCh38
NC_000002.11:g.128186129T>C , CM000664.1:g.128186129T>C	GRCh37
NC_000002.10:g.127902599T>C	NCBI36
NG_016323.1:g.15134T>C , LRG_599:g.15134T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.993T>C MANE Select	ENSP00000234071.4:p.Asn331=
ENST00000234071.7:c.993T>C	ENSP00000234071.3:p.Asn331=
ENST00000402125.2:c.317T>C
ENST00000409048.1:c.1095T>C	ENSP00000386679.1:p.Asn365=
NM_000312.3:c.993T>C , LRG_599t1:c.993T>C	NP_000303.1:p.Asn331=
XM_005263715.3:c.1176T>C	XP_005263772.1:p.Asn392=
XM_005263716.3:c.1158T>C	XP_005263773.1:p.Asn386=
XM_005263717.3:c.1056T>C	XP_005263774.1:p.Asn352=
XR_923313.1:n.1332-289A>G
XM_005263717.4:c.1056T>C	XP_005263774.1:p.Asn352=
XM_017004505.1:c.1236T>C	XP_016859994.1:p.Asn412=
XM_024453002.1:c.1338T>C	XP_024308770.1:p.Asn446=
XM_024453003.1:c.1278T>C	XP_024308771.1:p.Asn426=
XM_024453004.1:c.1176T>C	XP_024308772.1:p.Asn392=
XM_024453005.1:c.1158T>C	XP_024308773.1:p.Asn386=
XM_024453006.1:c.1095T>C	XP_024308774.1:p.Asn365=
XR_001739705.1:n.3607-289A>G
XR_923313.2:n.4043-289A>G
NM_000312.4:c.993T>C MANE Select	NP_000303.1:p.Asn331=
NM_001375602.1:c.1176T>C	NP_001362531.1:p.Asn392=
NM_001375603.1:c.1158T>C	NP_001362532.1:p.Asn386=
NM_001375604.1:c.1056T>C	NP_001362533.1:p.Asn352=
NM_001375605.1:c.1095T>C	NP_001362534.1:p.Asn365=
NM_001375606.1:c.1161T>C	NP_001362535.1:p.Asn387=
NM_001375607.1:c.1179T>C	NP_001362536.1:p.Asn393=
NM_001375608.1:c.936T>C	NP_001362537.1:p.Asn312=
NM_001375609.1:c.969T>C	NP_001362538.1:p.Asn323=
NM_001375610.1:c.987T>C	NP_001362539.1:p.Asn329=
NM_001375611.1:c.993T>C	NP_001362540.1:p.Asn331=
NM_001375613.1:c.993T>C	NP_001362542.1:p.Asn331=