Canonical Allele Identifier: CA1286883416

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426129C= , CM000664.2:g.127426129C=	GRCh38
NC_000002.11:g.128183705C= , CM000664.1:g.128183705C=	GRCh37
NC_000002.10:g.127900175C=	NCBI36
NG_016323.1:g.12710C= , LRG_599:g.12710C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.580C= MANE Select	ENSP00000234071.4:p.Arg194=
ENST00000234071.7:c.580C=	ENSP00000234071.3:p.Arg194=
ENST00000402125.2:c.121-2228C=
ENST00000409048.1:c.682C=	ENSP00000386679.1:p.Arg228=
ENST00000442644.5:c.523C=	ENSP00000411241.1:p.Arg175=
ENST00000464089.1:n.166C=
NM_000312.3:c.580C= , LRG_599t1:c.580C=	NP_000303.1:p.Arg194=
XM_005263715.3:c.763C=	XP_005263772.1:p.Arg255=
XM_005263716.3:c.745C=	XP_005263773.1:p.Arg249=
XM_005263717.3:c.643C=	XP_005263774.1:p.Arg215=
XM_005263717.4:c.643C=	XP_005263774.1:p.Arg215=
XM_017004505.1:c.823C=	XP_016859994.1:p.Arg275=
XM_024453002.1:c.925C=	XP_024308770.1:p.Arg309=
XM_024453003.1:c.865C=	XP_024308771.1:p.Arg289=
XM_024453004.1:c.763C=	XP_024308772.1:p.Arg255=
XM_024453005.1:c.745C=	XP_024308773.1:p.Arg249=
XM_024453006.1:c.682C=	XP_024308774.1:p.Arg228=
XR_923313.2:n.4456G=
NM_000312.4:c.580C= MANE Select	NP_000303.1:p.Arg194=
NM_001375602.1:c.763C=	NP_001362531.1:p.Arg255=
NM_001375603.1:c.745C=	NP_001362532.1:p.Arg249=
NM_001375604.1:c.643C=	NP_001362533.1:p.Arg215=
NM_001375605.1:c.682C=	NP_001362534.1:p.Arg228=
NM_001375606.1:c.748C=	NP_001362535.1:p.Arg250=
NM_001375607.1:c.766C=	NP_001362536.1:p.Arg256=
NM_001375608.1:c.523C=	NP_001362537.1:p.Arg175=
NM_001375609.1:c.556C=	NP_001362538.1:p.Arg186=
NM_001375610.1:c.574C=	NP_001362539.1:p.Arg192=
NM_001375611.1:c.580C=	NP_001362540.1:p.Arg194=
NM_001375613.1:c.580C=	NP_001362542.1:p.Arg194=