Canonical Allele Identifier: CA2739772592

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127423183A>C , CM000664.2:g.127423183A>C	GRCh38
NC_000002.11:g.128180759A>C , CM000664.1:g.128180759A>C	GRCh37
NC_000002.10:g.127897229A>C	NCBI36
NG_016323.1:g.9764A>C , LRG_599:g.9764A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.400+12A>C MANE Select	ENSP00000234071.4:n.400+12A>C
ENST00000234071.7:c.400+12A>C	ENSP00000234071.3:n.400+12A>C
ENST00000409048.1:c.412A>C	ENSP00000386679.1:p.Arg138=
ENST00000419985.5:c.*218A>C	ENSP00000392606.1:n.*218A>C
ENST00000442644.5:c.400+12A>C	ENSP00000411241.1:n.400+12A>C
NM_000312.3:c.400+12A>C , LRG_599t1:c.400+12A>C	NP_000303.1:n.400+12A>C
XM_005263715.3:c.583+12A>C	XP_005263772.1:n.583+12A>C
XM_005263716.3:c.475A>C	XP_005263773.1:p.Arg159=
XM_005263717.3:c.463+12A>C	XP_005263774.1:n.463+12A>C
XM_005263717.4:c.463+12A>C	XP_005263774.1:n.463+12A>C
XM_017004505.1:c.643+12A>C	XP_016859994.1:n.643+12A>C
XM_024453002.1:c.655A>C	XP_024308770.1:p.Arg219=
XM_024453003.1:c.595A>C	XP_024308771.1:p.Arg199=
XM_024453004.1:c.583+12A>C	XP_024308772.1:n.583+12A>C
XM_024453005.1:c.475A>C	XP_024308773.1:p.Arg159=
XM_024453006.1:c.412A>C	XP_024308774.1:p.Arg138=
NM_000312.4:c.400+12A>C MANE Select	NP_000303.1:n.400+12A>C
NM_001375602.1:c.583+12A>C	NP_001362531.1:n.583+12A>C
NM_001375603.1:c.475A>C	NP_001362532.1:p.Arg159=
NM_001375604.1:c.463+12A>C	NP_001362533.1:n.463+12A>C
NM_001375605.1:c.412A>C	NP_001362534.1:p.Arg138=
NM_001375606.1:c.567A>C	NP_001362535.1:p.Arg189Ser
NM_001375607.1:c.496A>C	NP_001362536.1:p.Arg166=
NM_001375608.1:c.400+12A>C	NP_001362537.1:n.400+12A>C
NM_001375609.1:c.376+12A>C	NP_001362538.1:n.376+12A>C
NM_001375610.1:c.394+12A>C	NP_001362539.1:n.394+12A>C
NM_001375611.1:c.400+12A>C	NP_001362540.1:n.400+12A>C
NM_001375613.1:c.400+12A>C	NP_001362542.1:n.400+12A>C