Canonical Allele Identifier: CA1286883431

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426164A= , CM000664.2:g.127426164A=	GRCh38
NC_000002.11:g.128183740A= , CM000664.1:g.128183740A=	GRCh37
NC_000002.10:g.127900210A=	NCBI36
NG_016323.1:g.12745A= , LRG_599:g.12745A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.615A= MANE Select	ENSP00000234071.4:p.Glu205=
ENST00000234071.7:c.615A=	ENSP00000234071.3:p.Glu205=
ENST00000402125.2:c.121-2193A=
ENST00000409048.1:c.717A=	ENSP00000386679.1:p.Glu239=
ENST00000464089.1:n.201A=
NM_000312.3:c.615A= , LRG_599t1:c.615A=	NP_000303.1:p.Glu205=
XM_005263715.3:c.798A=	XP_005263772.1:p.Glu266=
XM_005263716.3:c.780A=	XP_005263773.1:p.Glu260=
XM_005263717.3:c.678A=	XP_005263774.1:p.Glu226=
XM_005263717.4:c.678A=	XP_005263774.1:p.Glu226=
XM_017004505.1:c.858A=	XP_016859994.1:p.Glu286=
XM_024453002.1:c.960A=	XP_024308770.1:p.Glu320=
XM_024453003.1:c.900A=	XP_024308771.1:p.Glu300=
XM_024453004.1:c.798A=	XP_024308772.1:p.Glu266=
XM_024453005.1:c.780A=	XP_024308773.1:p.Glu260=
XM_024453006.1:c.717A=	XP_024308774.1:p.Glu239=
XR_923313.2:n.4421T=
NM_000312.4:c.615A= MANE Select	NP_000303.1:p.Glu205=
NM_001375602.1:c.798A=	NP_001362531.1:p.Glu266=
NM_001375603.1:c.780A=	NP_001362532.1:p.Glu260=
NM_001375604.1:c.678A=	NP_001362533.1:p.Glu226=
NM_001375605.1:c.717A=	NP_001362534.1:p.Glu239=
NM_001375606.1:c.783A=	NP_001362535.1:p.Glu261=
NM_001375607.1:c.801A=	NP_001362536.1:p.Glu267=
NM_001375608.1:c.558A=	NP_001362537.1:p.Glu186=
NM_001375609.1:c.591A=	NP_001362538.1:p.Glu197=
NM_001375610.1:c.609A=	NP_001362539.1:p.Glu203=
NM_001375611.1:c.615A=	NP_001362540.1:p.Glu205=
NM_001375613.1:c.615A=	NP_001362542.1:p.Glu205=