Canonical Allele Identifier: CA428617448

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128178977C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127421401C>A , CM000664.2:g.127421401C>A	GRCh38
NC_000002.11:g.128178977C>A , CM000664.1:g.128178977C>A	GRCh37
NC_000002.10:g.127895447C>A	NCBI36
NG_016323.1:g.7982C>A , LRG_599:g.7982C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.189C>A MANE Select	ENSP00000234071.4:p.Ile63=
ENST00000234071.7:c.189C>A	ENSP00000234071.3:p.Ile63=
ENST00000409048.1:c.189C>A	ENSP00000386679.1:p.Ile63=
ENST00000419985.5:c.154C>A	ENSP00000392606.1:p.Leu52Met
ENST00000427769.5:c.189C>A	ENSP00000406295.1:p.Ile63=
ENST00000429925.5:c.189C>A	ENSP00000412697.1:p.Ile63=
ENST00000431364.1:c.154C>A	ENSP00000391220.1:p.Leu52Met
ENST00000442644.5:c.189C>A	ENSP00000411241.1:p.Ile63=
ENST00000474030.5:n.272C>A
NM_000312.3:c.189C>A , LRG_599t1:c.189C>A	NP_000303.1:p.Ile63=
XM_005263715.3:c.372C>A	XP_005263772.1:p.Ile124=
XM_005263716.3:c.252C>A	XP_005263773.1:p.Ile84=
XM_005263717.3:c.252C>A	XP_005263774.1:p.Ile84=
XM_005263717.4:c.252C>A	XP_005263774.1:p.Ile84=
XM_017004505.1:c.432C>A	XP_016859994.1:p.Ile144=
XM_024453002.1:c.432C>A	XP_024308770.1:p.Ile144=
XM_024453003.1:c.372C>A	XP_024308771.1:p.Ile124=
XM_024453004.1:c.372C>A	XP_024308772.1:p.Ile124=
XM_024453005.1:c.252C>A	XP_024308773.1:p.Ile84=
XM_024453006.1:c.189C>A	XP_024308774.1:p.Ile63=
NM_000312.4:c.189C>A MANE Select	NP_000303.1:p.Ile63=
NM_001375602.1:c.372C>A	NP_001362531.1:p.Ile124=
NM_001375603.1:c.252C>A	NP_001362532.1:p.Ile84=
NM_001375604.1:c.252C>A	NP_001362533.1:p.Ile84=
NM_001375605.1:c.189C>A	NP_001362534.1:p.Ile63=
NM_001375606.1:c.252C>A	NP_001362535.1:p.Ile84=
NM_001375607.1:c.273C>A	NP_001362536.1:p.Ile91=
NM_001375608.1:c.189C>A	NP_001362537.1:p.Ile63=
NM_001375609.1:c.165C>A	NP_001362538.1:p.Ile55=
NM_001375610.1:c.183C>A	NP_001362539.1:p.Ile61=
NM_001375611.1:c.189C>A	NP_001362540.1:p.Ile63=
NM_001375613.1:c.189C>A	NP_001362542.1:p.Ile63=