Canonical Allele Identifier: CA1286883420

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426137C= , CM000664.2:g.127426137C=	GRCh38
NC_000002.11:g.128183713C= , CM000664.1:g.128183713C=	GRCh37
NC_000002.10:g.127900183C=	NCBI36
NG_016323.1:g.12718C= , LRG_599:g.12718C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.588C= MANE Select	ENSP00000234071.4:p.His196=
ENST00000234071.7:c.588C=	ENSP00000234071.3:p.His196=
ENST00000402125.2:c.121-2220C=
ENST00000409048.1:c.690C=	ENSP00000386679.1:p.His230=
ENST00000464089.1:n.174C=
NM_000312.3:c.588C= , LRG_599t1:c.588C=	NP_000303.1:p.His196=
XM_005263715.3:c.771C=	XP_005263772.1:p.His257=
XM_005263716.3:c.753C=	XP_005263773.1:p.His251=
XM_005263717.3:c.651C=	XP_005263774.1:p.His217=
XM_005263717.4:c.651C=	XP_005263774.1:p.His217=
XM_017004505.1:c.831C=	XP_016859994.1:p.His277=
XM_024453002.1:c.933C=	XP_024308770.1:p.His311=
XM_024453003.1:c.873C=	XP_024308771.1:p.His291=
XM_024453004.1:c.771C=	XP_024308772.1:p.His257=
XM_024453005.1:c.753C=	XP_024308773.1:p.His251=
XM_024453006.1:c.690C=	XP_024308774.1:p.His230=
XR_923313.2:n.4448G=
NM_000312.4:c.588C= MANE Select	NP_000303.1:p.His196=
NM_001375602.1:c.771C=	NP_001362531.1:p.His257=
NM_001375603.1:c.753C=	NP_001362532.1:p.His251=
NM_001375604.1:c.651C=	NP_001362533.1:p.His217=
NM_001375605.1:c.690C=	NP_001362534.1:p.His230=
NM_001375606.1:c.756C=	NP_001362535.1:p.His252=
NM_001375607.1:c.774C=	NP_001362536.1:p.His258=
NM_001375608.1:c.531C=	NP_001362537.1:p.His177=
NM_001375609.1:c.564C=	NP_001362538.1:p.His188=
NM_001375610.1:c.582C=	NP_001362539.1:p.His194=
NM_001375611.1:c.588C=	NP_001362540.1:p.His196=
NM_001375613.1:c.588C=	NP_001362542.1:p.His196=