Canonical Allele Identifier: CA428618328

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183764T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426188T>A , CM000664.2:g.127426188T>A	GRCh38
NC_000002.11:g.128183764T>A , CM000664.1:g.128183764T>A	GRCh37
NC_000002.10:g.127900234T>A	NCBI36
NG_016323.1:g.12769T>A , LRG_599:g.12769T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.639T>A MANE Select	ENSP00000234071.4:p.Ile213=
ENST00000234071.7:c.639T>A	ENSP00000234071.3:p.Ile213=
ENST00000402125.2:c.121-2169T>A
ENST00000409048.1:c.741T>A	ENSP00000386679.1:p.Ile247=
ENST00000464089.1:n.225T>A
NM_000312.3:c.639T>A , LRG_599t1:c.639T>A	NP_000303.1:p.Ile213=
XM_005263715.3:c.822T>A	XP_005263772.1:p.Ile274=
XM_005263716.3:c.804T>A	XP_005263773.1:p.Ile268=
XM_005263717.3:c.702T>A	XP_005263774.1:p.Ile234=
XM_005263717.4:c.702T>A	XP_005263774.1:p.Ile234=
XM_017004505.1:c.882T>A	XP_016859994.1:p.Ile294=
XM_024453002.1:c.984T>A	XP_024308770.1:p.Ile328=
XM_024453003.1:c.924T>A	XP_024308771.1:p.Ile308=
XM_024453004.1:c.822T>A	XP_024308772.1:p.Ile274=
XM_024453005.1:c.804T>A	XP_024308773.1:p.Ile268=
XM_024453006.1:c.741T>A	XP_024308774.1:p.Ile247=
XR_923313.2:n.4397A>T
NM_000312.4:c.639T>A MANE Select	NP_000303.1:p.Ile213=
NM_001375602.1:c.822T>A	NP_001362531.1:p.Ile274=
NM_001375603.1:c.804T>A	NP_001362532.1:p.Ile268=
NM_001375604.1:c.702T>A	NP_001362533.1:p.Ile234=
NM_001375605.1:c.741T>A	NP_001362534.1:p.Ile247=
NM_001375606.1:c.807T>A	NP_001362535.1:p.Ile269=
NM_001375607.1:c.825T>A	NP_001362536.1:p.Ile275=
NM_001375608.1:c.582T>A	NP_001362537.1:p.Ile194=
NM_001375609.1:c.615T>A	NP_001362538.1:p.Ile205=
NM_001375610.1:c.633T>A	NP_001362539.1:p.Ile211=
NM_001375611.1:c.639T>A	NP_001362540.1:p.Ile213=
NM_001375613.1:c.639T>A	NP_001362542.1:p.Ile213=