Canonical Allele Identifier: CA1286883414

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426126A= , CM000664.2:g.127426126A=	GRCh38
NC_000002.11:g.128183702A= , CM000664.1:g.128183702A=	GRCh37
NC_000002.10:g.127900172A=	NCBI36
NG_016323.1:g.12707A= , LRG_599:g.12707A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.577A= MANE Select	ENSP00000234071.4:p.Lys193=
ENST00000234071.7:c.577A=	ENSP00000234071.3:p.Lys193=
ENST00000402125.2:c.121-2231A=
ENST00000409048.1:c.679A=	ENSP00000386679.1:p.Lys227=
ENST00000442644.5:c.520A=	ENSP00000411241.1:p.Lys174=
ENST00000464089.1:n.163A=
NM_000312.3:c.577A= , LRG_599t1:c.577A=	NP_000303.1:p.Lys193=
XM_005263715.3:c.760A=	XP_005263772.1:p.Lys254=
XM_005263716.3:c.742A=	XP_005263773.1:p.Lys248=
XM_005263717.3:c.640A=	XP_005263774.1:p.Lys214=
XM_005263717.4:c.640A=	XP_005263774.1:p.Lys214=
XM_017004505.1:c.820A=	XP_016859994.1:p.Lys274=
XM_024453002.1:c.922A=	XP_024308770.1:p.Lys308=
XM_024453003.1:c.862A=	XP_024308771.1:p.Lys288=
XM_024453004.1:c.760A=	XP_024308772.1:p.Lys254=
XM_024453005.1:c.742A=	XP_024308773.1:p.Lys248=
XM_024453006.1:c.679A=	XP_024308774.1:p.Lys227=
XR_923313.2:n.4459T=
NM_000312.4:c.577A= MANE Select	NP_000303.1:p.Lys193=
NM_001375602.1:c.760A=	NP_001362531.1:p.Lys254=
NM_001375603.1:c.742A=	NP_001362532.1:p.Lys248=
NM_001375604.1:c.640A=	NP_001362533.1:p.Lys214=
NM_001375605.1:c.679A=	NP_001362534.1:p.Lys227=
NM_001375606.1:c.745A=	NP_001362535.1:p.Lys249=
NM_001375607.1:c.763A=	NP_001362536.1:p.Lys255=
NM_001375608.1:c.520A=	NP_001362537.1:p.Lys174=
NM_001375609.1:c.553A=	NP_001362538.1:p.Lys185=
NM_001375610.1:c.571A=	NP_001362539.1:p.Lys191=
NM_001375611.1:c.577A=	NP_001362540.1:p.Lys193=
NM_001375613.1:c.577A=	NP_001362542.1:p.Lys193=