Canonical Allele Identifier: CA428618263

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183722A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426146A>T , CM000664.2:g.127426146A>T	GRCh38
NC_000002.11:g.128183722A>T , CM000664.1:g.128183722A>T	GRCh37
NC_000002.10:g.127900192A>T	NCBI36
NG_016323.1:g.12727A>T , LRG_599:g.12727A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.597A>T MANE Select	ENSP00000234071.4:p.Arg199=
ENST00000234071.7:c.597A>T	ENSP00000234071.3:p.Arg199=
ENST00000402125.2:c.121-2211A>T
ENST00000409048.1:c.699A>T	ENSP00000386679.1:p.Arg233=
ENST00000464089.1:n.183A>T
NM_000312.3:c.597A>T , LRG_599t1:c.597A>T	NP_000303.1:p.Arg199=
XM_005263715.3:c.780A>T	XP_005263772.1:p.Arg260=
XM_005263716.3:c.762A>T	XP_005263773.1:p.Arg254=
XM_005263717.3:c.660A>T	XP_005263774.1:p.Arg220=
XM_005263717.4:c.660A>T	XP_005263774.1:p.Arg220=
XM_017004505.1:c.840A>T	XP_016859994.1:p.Arg280=
XM_024453002.1:c.942A>T	XP_024308770.1:p.Arg314=
XM_024453003.1:c.882A>T	XP_024308771.1:p.Arg294=
XM_024453004.1:c.780A>T	XP_024308772.1:p.Arg260=
XM_024453005.1:c.762A>T	XP_024308773.1:p.Arg254=
XM_024453006.1:c.699A>T	XP_024308774.1:p.Arg233=
XR_923313.2:n.4439T>A
NM_000312.4:c.597A>T MANE Select	NP_000303.1:p.Arg199=
NM_001375602.1:c.780A>T	NP_001362531.1:p.Arg260=
NM_001375603.1:c.762A>T	NP_001362532.1:p.Arg254=
NM_001375604.1:c.660A>T	NP_001362533.1:p.Arg220=
NM_001375605.1:c.699A>T	NP_001362534.1:p.Arg233=
NM_001375606.1:c.765A>T	NP_001362535.1:p.Arg255=
NM_001375607.1:c.783A>T	NP_001362536.1:p.Arg261=
NM_001375608.1:c.540A>T	NP_001362537.1:p.Arg180=
NM_001375609.1:c.573A>T	NP_001362538.1:p.Arg191=
NM_001375610.1:c.591A>T	NP_001362539.1:p.Arg197=
NM_001375611.1:c.597A>T	NP_001362540.1:p.Arg199=
NM_001375613.1:c.597A>T	NP_001362542.1:p.Arg199=