Canonical Allele Identifier: CA1286883404

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426110G= , CM000664.2:g.127426110G=	GRCh38
NC_000002.11:g.128183686G= , CM000664.1:g.128183686G=	GRCh37
NC_000002.10:g.127900156G=	NCBI36
NG_016323.1:g.12691G= , LRG_599:g.12691G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.561G= MANE Select	ENSP00000234071.4:p.Trp187=
ENST00000234071.7:c.561G=	ENSP00000234071.3:p.Trp187=
ENST00000402125.2:c.121-2247G=
ENST00000409048.1:c.663G=	ENSP00000386679.1:p.Trp221=
ENST00000442644.5:c.504G=	ENSP00000411241.1:p.Trp168=
ENST00000464089.1:n.147G=
NM_000312.3:c.561G= , LRG_599t1:c.561G=	NP_000303.1:p.Trp187=
XM_005263715.3:c.744G=	XP_005263772.1:p.Trp248=
XM_005263716.3:c.726G=	XP_005263773.1:p.Trp242=
XM_005263717.3:c.624G=	XP_005263774.1:p.Trp208=
XM_005263717.4:c.624G=	XP_005263774.1:p.Trp208=
XM_017004505.1:c.804G=	XP_016859994.1:p.Trp268=
XM_024453002.1:c.906G=	XP_024308770.1:p.Trp302=
XM_024453003.1:c.846G=	XP_024308771.1:p.Trp282=
XM_024453004.1:c.744G=	XP_024308772.1:p.Trp248=
XM_024453005.1:c.726G=	XP_024308773.1:p.Trp242=
XM_024453006.1:c.663G=	XP_024308774.1:p.Trp221=
XR_923313.2:n.4475C=
NM_000312.4:c.561G= MANE Select	NP_000303.1:p.Trp187=
NM_001375602.1:c.744G=	NP_001362531.1:p.Trp248=
NM_001375603.1:c.726G=	NP_001362532.1:p.Trp242=
NM_001375604.1:c.624G=	NP_001362533.1:p.Trp208=
NM_001375605.1:c.663G=	NP_001362534.1:p.Trp221=
NM_001375606.1:c.729G=	NP_001362535.1:p.Trp243=
NM_001375607.1:c.747G=	NP_001362536.1:p.Trp249=
NM_001375608.1:c.504G=	NP_001362537.1:p.Trp168=
NM_001375609.1:c.537G=	NP_001362538.1:p.Trp179=
NM_001375610.1:c.555G=	NP_001362539.1:p.Trp185=
NM_001375611.1:c.561G=	NP_001362540.1:p.Trp187=
NM_001375613.1:c.561G=	NP_001362542.1:p.Trp187=