Canonical Allele Identifier: CA1286884600

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428714T= , CM000664.2:g.127428714T=	GRCh38
NC_000002.11:g.128186290T= , CM000664.1:g.128186290T=	GRCh37
NC_000002.10:g.127902760T=	NCBI36
NG_016323.1:g.15295T= , LRG_599:g.15295T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1154T= MANE Select	ENSP00000234071.4:p.Met385=
ENST00000234071.7:c.1154T=	ENSP00000234071.3:p.Met385=
ENST00000402125.2:c.478T=
ENST00000409048.1:c.1256T=	ENSP00000386679.1:p.Met419=
NM_000312.3:c.1154T= , LRG_599t1:c.1154T=	NP_000303.1:p.Met385=
XM_005263715.3:c.1337T=	XP_005263772.1:p.Met446=
XM_005263716.3:c.1319T=	XP_005263773.1:p.Met440=
XM_005263717.3:c.1217T=	XP_005263774.1:p.Met406=
XR_923313.1:n.1332-450A=
XM_005263717.4:c.1217T=	XP_005263774.1:p.Met406=
XM_017004505.1:c.1397T=	XP_016859994.1:p.Met466=
XM_024453002.1:c.1499T=	XP_024308770.1:p.Met500=
XM_024453003.1:c.1439T=	XP_024308771.1:p.Met480=
XM_024453004.1:c.1337T=	XP_024308772.1:p.Met446=
XM_024453005.1:c.1319T=	XP_024308773.1:p.Met440=
XM_024453006.1:c.1256T=	XP_024308774.1:p.Met419=
XR_001739705.1:n.3607-450A=
XR_923313.2:n.4043-450A=
NM_000312.4:c.1154T= MANE Select	NP_000303.1:p.Met385=
NM_001375602.1:c.1337T=	NP_001362531.1:p.Met446=
NM_001375603.1:c.1319T=	NP_001362532.1:p.Met440=
NM_001375604.1:c.1217T=	NP_001362533.1:p.Met406=
NM_001375605.1:c.1256T=	NP_001362534.1:p.Met419=
NM_001375606.1:c.1322T=	NP_001362535.1:p.Met441=
NM_001375607.1:c.1340T=	NP_001362536.1:p.Met447=
NM_001375608.1:c.1097T=	NP_001362537.1:p.Met366=
NM_001375609.1:c.1130T=	NP_001362538.1:p.Met377=
NM_001375610.1:c.1148T=	NP_001362539.1:p.Met383=
NM_001375611.1:c.1154T=	NP_001362540.1:p.Met385=
NM_001375613.1:c.1154T=	NP_001362542.1:p.Met385=