Canonical Allele Identifier: CA428618190

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183678A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426102A>C , CM000664.2:g.127426102A>C	GRCh38
NC_000002.11:g.128183678A>C , CM000664.1:g.128183678A>C	GRCh37
NC_000002.10:g.127900148A>C	NCBI36
NG_016323.1:g.12683A>C , LRG_599:g.12683A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.553A>C MANE Select	ENSP00000234071.4:p.Arg185=
ENST00000234071.7:c.553A>C	ENSP00000234071.3:p.Arg185=
ENST00000402125.2:c.121-2255A>C
ENST00000409048.1:c.655A>C	ENSP00000386679.1:p.Arg219=
ENST00000442644.5:c.496A>C	ENSP00000411241.1:p.Arg166=
ENST00000464089.1:n.139A>C
NM_000312.3:c.553A>C , LRG_599t1:c.553A>C	NP_000303.1:p.Arg185=
XM_005263715.3:c.736A>C	XP_005263772.1:p.Arg246=
XM_005263716.3:c.718A>C	XP_005263773.1:p.Arg240=
XM_005263717.3:c.616A>C	XP_005263774.1:p.Arg206=
XM_005263717.4:c.616A>C	XP_005263774.1:p.Arg206=
XM_017004505.1:c.796A>C	XP_016859994.1:p.Arg266=
XM_024453002.1:c.898A>C	XP_024308770.1:p.Arg300=
XM_024453003.1:c.838A>C	XP_024308771.1:p.Arg280=
XM_024453004.1:c.736A>C	XP_024308772.1:p.Arg246=
XM_024453005.1:c.718A>C	XP_024308773.1:p.Arg240=
XM_024453006.1:c.655A>C	XP_024308774.1:p.Arg219=
XR_923313.2:n.4483T>G
NM_000312.4:c.553A>C MANE Select	NP_000303.1:p.Arg185=
NM_001375602.1:c.736A>C	NP_001362531.1:p.Arg246=
NM_001375603.1:c.718A>C	NP_001362532.1:p.Arg240=
NM_001375604.1:c.616A>C	NP_001362533.1:p.Arg206=
NM_001375605.1:c.655A>C	NP_001362534.1:p.Arg219=
NM_001375606.1:c.721A>C	NP_001362535.1:p.Arg241=
NM_001375607.1:c.739A>C	NP_001362536.1:p.Arg247=
NM_001375608.1:c.496A>C	NP_001362537.1:p.Arg166=
NM_001375609.1:c.529A>C	NP_001362538.1:p.Arg177=
NM_001375610.1:c.547A>C	NP_001362539.1:p.Arg183=
NM_001375611.1:c.553A>C	NP_001362540.1:p.Arg185=
NM_001375613.1:c.553A>C	NP_001362542.1:p.Arg185=