Canonical Allele Identifier: CA1286884429

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428364T= , CM000664.2:g.127428364T=	GRCh38
NC_000002.11:g.128185940T= , CM000664.1:g.128185940T=	GRCh37
NC_000002.10:g.127902410T=	NCBI36
NG_016323.1:g.14945T= , LRG_599:g.14945T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.804T= MANE Select	ENSP00000234071.4:p.Tyr268=
ENST00000234071.7:c.804T=	ENSP00000234071.3:p.Tyr268=
ENST00000402125.2:c.128T=
ENST00000409048.1:c.906T=	ENSP00000386679.1:p.Tyr302=
NM_000312.3:c.804T= , LRG_599t1:c.804T=	NP_000303.1:p.Tyr268=
XM_005263715.3:c.987T=	XP_005263772.1:p.Tyr329=
XM_005263716.3:c.969T=	XP_005263773.1:p.Tyr323=
XM_005263717.3:c.867T=	XP_005263774.1:p.Tyr289=
XR_923313.1:n.1332-100A=
XM_005263717.4:c.867T=	XP_005263774.1:p.Tyr289=
XM_017004505.1:c.1047T=	XP_016859994.1:p.Tyr349=
XM_024453002.1:c.1149T=	XP_024308770.1:p.Tyr383=
XM_024453003.1:c.1089T=	XP_024308771.1:p.Tyr363=
XM_024453004.1:c.987T=	XP_024308772.1:p.Tyr329=
XM_024453005.1:c.969T=	XP_024308773.1:p.Tyr323=
XM_024453006.1:c.906T=	XP_024308774.1:p.Tyr302=
XR_001739705.1:n.3607-100A=
XR_923313.2:n.4043-100A=
NM_000312.4:c.804T= MANE Select	NP_000303.1:p.Tyr268=
NM_001375602.1:c.987T=	NP_001362531.1:p.Tyr329=
NM_001375603.1:c.969T=	NP_001362532.1:p.Tyr323=
NM_001375604.1:c.867T=	NP_001362533.1:p.Tyr289=
NM_001375605.1:c.906T=	NP_001362534.1:p.Tyr302=
NM_001375606.1:c.972T=	NP_001362535.1:p.Tyr324=
NM_001375607.1:c.990T=	NP_001362536.1:p.Tyr330=
NM_001375608.1:c.747T=	NP_001362537.1:p.Tyr249=
NM_001375609.1:c.780T=	NP_001362538.1:p.Tyr260=
NM_001375610.1:c.798T=	NP_001362539.1:p.Tyr266=
NM_001375611.1:c.804T=	NP_001362540.1:p.Tyr268=
NM_001375613.1:c.804T=	NP_001362542.1:p.Tyr268=