Canonical Allele Identifier: CA428618203

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183689G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426113G>A , CM000664.2:g.127426113G>A	GRCh38
NC_000002.11:g.128183689G>A , CM000664.1:g.128183689G>A	GRCh37
NC_000002.10:g.127900159G>A	NCBI36
NG_016323.1:g.12694G>A , LRG_599:g.12694G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.564G>A MANE Select	ENSP00000234071.4:p.Lys188=
ENST00000234071.7:c.564G>A	ENSP00000234071.3:p.Lys188=
ENST00000402125.2:c.121-2244G>A
ENST00000409048.1:c.666G>A	ENSP00000386679.1:p.Lys222=
ENST00000442644.5:c.507G>A	ENSP00000411241.1:p.Lys169=
ENST00000464089.1:n.150G>A
NM_000312.3:c.564G>A , LRG_599t1:c.564G>A	NP_000303.1:p.Lys188=
XM_005263715.3:c.747G>A	XP_005263772.1:p.Lys249=
XM_005263716.3:c.729G>A	XP_005263773.1:p.Lys243=
XM_005263717.3:c.627G>A	XP_005263774.1:p.Lys209=
XM_005263717.4:c.627G>A	XP_005263774.1:p.Lys209=
XM_017004505.1:c.807G>A	XP_016859994.1:p.Lys269=
XM_024453002.1:c.909G>A	XP_024308770.1:p.Lys303=
XM_024453003.1:c.849G>A	XP_024308771.1:p.Lys283=
XM_024453004.1:c.747G>A	XP_024308772.1:p.Lys249=
XM_024453005.1:c.729G>A	XP_024308773.1:p.Lys243=
XM_024453006.1:c.666G>A	XP_024308774.1:p.Lys222=
XR_923313.2:n.4472C>T
NM_000312.4:c.564G>A MANE Select	NP_000303.1:p.Lys188=
NM_001375602.1:c.747G>A	NP_001362531.1:p.Lys249=
NM_001375603.1:c.729G>A	NP_001362532.1:p.Lys243=
NM_001375604.1:c.627G>A	NP_001362533.1:p.Lys209=
NM_001375605.1:c.666G>A	NP_001362534.1:p.Lys222=
NM_001375606.1:c.732G>A	NP_001362535.1:p.Lys244=
NM_001375607.1:c.750G>A	NP_001362536.1:p.Lys250=
NM_001375608.1:c.507G>A	NP_001362537.1:p.Lys169=
NM_001375609.1:c.540G>A	NP_001362538.1:p.Lys180=
NM_001375610.1:c.558G>A	NP_001362539.1:p.Lys186=
NM_001375611.1:c.564G>A	NP_001362540.1:p.Lys188=
NM_001375613.1:c.564G>A	NP_001362542.1:p.Lys188=