Canonical Allele Identifier: CA428872311

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186327C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428751C>G , CM000664.2:g.127428751C>G	GRCh38
NC_000002.11:g.128186327C>G , CM000664.1:g.128186327C>G	GRCh37
NC_000002.10:g.127902797C>G	NCBI36
NG_016323.1:g.15332C>G , LRG_599:g.15332C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1191C>G MANE Select	ENSP00000234071.4:p.Ala397=
ENST00000234071.7:c.1191C>G	ENSP00000234071.3:p.Ala397=
ENST00000402125.2:c.515C>G
ENST00000409048.1:c.1293C>G	ENSP00000386679.1:p.Ala431=
NM_000312.3:c.1191C>G , LRG_599t1:c.1191C>G	NP_000303.1:p.Ala397=
XM_005263715.3:c.1374C>G	XP_005263772.1:p.Ala458=
XM_005263716.3:c.1356C>G	XP_005263773.1:p.Ala452=
XM_005263717.3:c.1254C>G	XP_005263774.1:p.Ala418=
XR_923313.1:n.1332-487G>C
XM_005263717.4:c.1254C>G	XP_005263774.1:p.Ala418=
XM_017004505.1:c.1434C>G	XP_016859994.1:p.Ala478=
XM_024453002.1:c.1536C>G	XP_024308770.1:p.Ala512=
XM_024453003.1:c.1476C>G	XP_024308771.1:p.Ala492=
XM_024453004.1:c.1374C>G	XP_024308772.1:p.Ala458=
XM_024453005.1:c.1356C>G	XP_024308773.1:p.Ala452=
XM_024453006.1:c.1293C>G	XP_024308774.1:p.Ala431=
XR_001739705.1:n.3607-487G>C
XR_923313.2:n.4043-487G>C
NM_000312.4:c.1191C>G MANE Select	NP_000303.1:p.Ala397=
NM_001375602.1:c.1374C>G	NP_001362531.1:p.Ala458=
NM_001375603.1:c.1356C>G	NP_001362532.1:p.Ala452=
NM_001375604.1:c.1254C>G	NP_001362533.1:p.Ala418=
NM_001375605.1:c.1293C>G	NP_001362534.1:p.Ala431=
NM_001375606.1:c.1359C>G	NP_001362535.1:p.Ala453=
NM_001375607.1:c.1377C>G	NP_001362536.1:p.Ala459=
NM_001375608.1:c.1134C>G	NP_001362537.1:p.Ala378=
NM_001375609.1:c.1167C>G	NP_001362538.1:p.Ala389=
NM_001375610.1:c.1185C>G	NP_001362539.1:p.Ala395=
NM_001375611.1:c.1191C>G	NP_001362540.1:p.Ala397=
NM_001375613.1:c.1191C>G	NP_001362542.1:p.Ala397=