Canonical Allele Identifier: CA428618355

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183785G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426209G>T , CM000664.2:g.127426209G>T	GRCh38
NC_000002.11:g.128183785G>T , CM000664.1:g.128183785G>T	GRCh37
NC_000002.10:g.127900255G>T	NCBI36
NG_016323.1:g.12790G>T , LRG_599:g.12790G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.660G>T MANE Select	ENSP00000234071.4:p.Arg220=
ENST00000234071.7:c.660G>T	ENSP00000234071.3:p.Arg220=
ENST00000402125.2:c.121-2148G>T
ENST00000409048.1:c.762G>T	ENSP00000386679.1:p.Arg254=
ENST00000464089.1:n.246G>T
NM_000312.3:c.660G>T , LRG_599t1:c.660G>T	NP_000303.1:p.Arg220=
XM_005263715.3:c.843G>T	XP_005263772.1:p.Arg281=
XM_005263716.3:c.825G>T	XP_005263773.1:p.Arg275=
XM_005263717.3:c.723G>T	XP_005263774.1:p.Arg241=
XM_005263717.4:c.723G>T	XP_005263774.1:p.Arg241=
XM_017004505.1:c.903G>T	XP_016859994.1:p.Arg301=
XM_024453002.1:c.1005G>T	XP_024308770.1:p.Arg335=
XM_024453003.1:c.945G>T	XP_024308771.1:p.Arg315=
XM_024453004.1:c.843G>T	XP_024308772.1:p.Arg281=
XM_024453005.1:c.825G>T	XP_024308773.1:p.Arg275=
XM_024453006.1:c.762G>T	XP_024308774.1:p.Arg254=
XR_923313.2:n.4376C>A
NM_000312.4:c.660G>T MANE Select	NP_000303.1:p.Arg220=
NM_001375602.1:c.843G>T	NP_001362531.1:p.Arg281=
NM_001375603.1:c.825G>T	NP_001362532.1:p.Arg275=
NM_001375604.1:c.723G>T	NP_001362533.1:p.Arg241=
NM_001375605.1:c.762G>T	NP_001362534.1:p.Arg254=
NM_001375606.1:c.828G>T	NP_001362535.1:p.Arg276=
NM_001375607.1:c.846G>T	NP_001362536.1:p.Arg282=
NM_001375608.1:c.603G>T	NP_001362537.1:p.Arg201=
NM_001375609.1:c.636G>T	NP_001362538.1:p.Arg212=
NM_001375610.1:c.654G>T	NP_001362539.1:p.Arg218=
NM_001375611.1:c.660G>T	NP_001362540.1:p.Arg220=
NM_001375613.1:c.660G>T	NP_001362542.1:p.Arg220=