Canonical Allele Identifier: CA1286882054

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127423190T= , CM000664.2:g.127423190T=	GRCh38
NC_000002.11:g.128180766T= , CM000664.1:g.128180766T=	GRCh37
NC_000002.10:g.127897236T=	NCBI36
NG_016323.1:g.9771T= , LRG_599:g.9771T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.400+19T= MANE Select	ENSP00000234071.4:n.400+19T=
ENST00000234071.7:c.400+19T=	ENSP00000234071.3:n.400+19T=
ENST00000409048.1:c.419T=	ENSP00000386679.1:p.Met140=
ENST00000419985.5:c.*225T=	ENSP00000392606.1:n.*225T=
ENST00000442644.5:c.400+19T=	ENSP00000411241.1:n.400+19T=
NM_000312.3:c.400+19T= , LRG_599t1:c.400+19T=	NP_000303.1:n.400+19T=
XM_005263715.3:c.583+19T=	XP_005263772.1:n.583+19T=
XM_005263716.3:c.482T=	XP_005263773.1:p.Met161=
XM_005263717.3:c.463+19T=	XP_005263774.1:n.463+19T=
XM_005263717.4:c.463+19T=	XP_005263774.1:n.463+19T=
XM_017004505.1:c.643+19T=	XP_016859994.1:n.643+19T=
XM_024453002.1:c.662T=	XP_024308770.1:p.Met221=
XM_024453003.1:c.602T=	XP_024308771.1:p.Met201=
XM_024453004.1:c.583+19T=	XP_024308772.1:n.583+19T=
XM_024453005.1:c.482T=	XP_024308773.1:p.Met161=
XM_024453006.1:c.419T=	XP_024308774.1:p.Met140=
NM_000312.4:c.400+19T= MANE Select	NP_000303.1:n.400+19T=
NM_001375602.1:c.583+19T=	NP_001362531.1:n.583+19T=
NM_001375603.1:c.482T=	NP_001362532.1:p.Met161=
NM_001375604.1:c.463+19T=	NP_001362533.1:n.463+19T=
NM_001375605.1:c.419T=	NP_001362534.1:p.Met140=
NM_001375606.1:c.568+6T=	NP_001362535.1:n.568+6T=
NM_001375607.1:c.503T=	NP_001362536.1:p.Met168=
NM_001375608.1:c.400+19T=	NP_001362537.1:n.400+19T=
NM_001375609.1:c.376+19T=	NP_001362538.1:n.376+19T=
NM_001375610.1:c.394+19T=	NP_001362539.1:n.394+19T=
NM_001375611.1:c.400+19T=	NP_001362540.1:n.400+19T=
NM_001375613.1:c.400+19T=	NP_001362542.1:n.400+19T=