Canonical Allele Identifier: CA1286884547

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428607G= , CM000664.2:g.127428607G=	GRCh38
NC_000002.11:g.128186183G= , CM000664.1:g.128186183G=	GRCh37
NC_000002.10:g.127902653G=	NCBI36
NG_016323.1:g.15188G= , LRG_599:g.15188G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1047G= MANE Select	ENSP00000234071.4:p.Glu349=
ENST00000234071.7:c.1047G=	ENSP00000234071.3:p.Glu349=
ENST00000402125.2:c.371G=
ENST00000409048.1:c.1149G=	ENSP00000386679.1:p.Glu383=
NM_000312.3:c.1047G= , LRG_599t1:c.1047G=	NP_000303.1:p.Glu349=
XM_005263715.3:c.1230G=	XP_005263772.1:p.Glu410=
XM_005263716.3:c.1212G=	XP_005263773.1:p.Glu404=
XM_005263717.3:c.1110G=	XP_005263774.1:p.Glu370=
XR_923313.1:n.1332-343C=
XM_005263717.4:c.1110G=	XP_005263774.1:p.Glu370=
XM_017004505.1:c.1290G=	XP_016859994.1:p.Glu430=
XM_024453002.1:c.1392G=	XP_024308770.1:p.Glu464=
XM_024453003.1:c.1332G=	XP_024308771.1:p.Glu444=
XM_024453004.1:c.1230G=	XP_024308772.1:p.Glu410=
XM_024453005.1:c.1212G=	XP_024308773.1:p.Glu404=
XM_024453006.1:c.1149G=	XP_024308774.1:p.Glu383=
XR_001739705.1:n.3607-343C=
XR_923313.2:n.4043-343C=
NM_000312.4:c.1047G= MANE Select	NP_000303.1:p.Glu349=
NM_001375602.1:c.1230G=	NP_001362531.1:p.Glu410=
NM_001375603.1:c.1212G=	NP_001362532.1:p.Glu404=
NM_001375604.1:c.1110G=	NP_001362533.1:p.Glu370=
NM_001375605.1:c.1149G=	NP_001362534.1:p.Glu383=
NM_001375606.1:c.1215G=	NP_001362535.1:p.Glu405=
NM_001375607.1:c.1233G=	NP_001362536.1:p.Glu411=
NM_001375608.1:c.990G=	NP_001362537.1:p.Glu330=
NM_001375609.1:c.1023G=	NP_001362538.1:p.Glu341=
NM_001375610.1:c.1041G=	NP_001362539.1:p.Glu347=
NM_001375611.1:c.1047G=	NP_001362540.1:p.Glu349=
NM_001375613.1:c.1047G=	NP_001362542.1:p.Glu349=