Canonical Allele Identifier: CA1286883419

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426132A= , CM000664.2:g.127426132A=	GRCh38
NC_000002.11:g.128183708A= , CM000664.1:g.128183708A=	GRCh37
NC_000002.10:g.127900178A=	NCBI36
NG_016323.1:g.12713A= , LRG_599:g.12713A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.583A= MANE Select	ENSP00000234071.4:p.Ser195=
ENST00000234071.7:c.583A=	ENSP00000234071.3:p.Ser195=
ENST00000402125.2:c.121-2225A=
ENST00000409048.1:c.685A=	ENSP00000386679.1:p.Ser229=
ENST00000464089.1:n.169A=
NM_000312.3:c.583A= , LRG_599t1:c.583A=	NP_000303.1:p.Ser195=
XM_005263715.3:c.766A=	XP_005263772.1:p.Ser256=
XM_005263716.3:c.748A=	XP_005263773.1:p.Ser250=
XM_005263717.3:c.646A=	XP_005263774.1:p.Ser216=
XM_005263717.4:c.646A=	XP_005263774.1:p.Ser216=
XM_017004505.1:c.826A=	XP_016859994.1:p.Ser276=
XM_024453002.1:c.928A=	XP_024308770.1:p.Ser310=
XM_024453003.1:c.868A=	XP_024308771.1:p.Ser290=
XM_024453004.1:c.766A=	XP_024308772.1:p.Ser256=
XM_024453005.1:c.748A=	XP_024308773.1:p.Ser250=
XM_024453006.1:c.685A=	XP_024308774.1:p.Ser229=
XR_923313.2:n.4453T=
NM_000312.4:c.583A= MANE Select	NP_000303.1:p.Ser195=
NM_001375602.1:c.766A=	NP_001362531.1:p.Ser256=
NM_001375603.1:c.748A=	NP_001362532.1:p.Ser250=
NM_001375604.1:c.646A=	NP_001362533.1:p.Ser216=
NM_001375605.1:c.685A=	NP_001362534.1:p.Ser229=
NM_001375606.1:c.751A=	NP_001362535.1:p.Ser251=
NM_001375607.1:c.769A=	NP_001362536.1:p.Ser257=
NM_001375608.1:c.526A=	NP_001362537.1:p.Ser176=
NM_001375609.1:c.559A=	NP_001362538.1:p.Ser187=
NM_001375610.1:c.577A=	NP_001362539.1:p.Ser193=
NM_001375611.1:c.583A=	NP_001362540.1:p.Ser195=
NM_001375613.1:c.583A=	NP_001362542.1:p.Ser195=