Canonical Allele Identifier: CA348405168

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186109C>G (hg19) ; chr2:g.127428533C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428533C>G , CM000664.2:g.127428533C>G	GRCh38
NC_000002.11:g.128186109C>G , CM000664.1:g.128186109C>G	GRCh37
NC_000002.10:g.127902579C>G	NCBI36
NG_016323.1:g.15114C>G , LRG_599:g.15114C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.973C>G MANE Select	ENSP00000234071.4:p.Leu325Val
ENST00000234071.7:c.973C>G	ENSP00000234071.3:p.Leu325Val
ENST00000402125.2:c.297C>G
ENST00000409048.1:c.1075C>G	ENSP00000386679.1:p.Leu359Val
NM_000312.3:c.973C>G , LRG_599t1:c.973C>G	NP_000303.1:p.Leu325Val
XM_005263715.3:c.1156C>G	XP_005263772.1:p.Leu386Val
XM_005263716.3:c.1138C>G	XP_005263773.1:p.Leu380Val
XM_005263717.3:c.1036C>G	XP_005263774.1:p.Leu346Val
XR_923313.1:n.1332-269G>C
XM_005263717.4:c.1036C>G	XP_005263774.1:p.Leu346Val
XM_017004505.1:c.1216C>G	XP_016859994.1:p.Leu406Val
XM_024453002.1:c.1318C>G	XP_024308770.1:p.Leu440Val
XM_024453003.1:c.1258C>G	XP_024308771.1:p.Leu420Val
XM_024453004.1:c.1156C>G	XP_024308772.1:p.Leu386Val
XM_024453005.1:c.1138C>G	XP_024308773.1:p.Leu380Val
XM_024453006.1:c.1075C>G	XP_024308774.1:p.Leu359Val
XR_001739705.1:n.3607-269G>C
XR_923313.2:n.4043-269G>C
NM_000312.4:c.973C>G MANE Select	NP_000303.1:p.Leu325Val
NM_001375602.1:c.1156C>G	NP_001362531.1:p.Leu386Val
NM_001375603.1:c.1138C>G	NP_001362532.1:p.Leu380Val
NM_001375604.1:c.1036C>G	NP_001362533.1:p.Leu346Val
NM_001375605.1:c.1075C>G	NP_001362534.1:p.Leu359Val
NM_001375606.1:c.1141C>G	NP_001362535.1:p.Leu381Val
NM_001375607.1:c.1159C>G	NP_001362536.1:p.Leu387Val
NM_001375608.1:c.916C>G	NP_001362537.1:p.Leu306Val
NM_001375609.1:c.949C>G	NP_001362538.1:p.Leu317Val
NM_001375610.1:c.967C>G	NP_001362539.1:p.Leu323Val
NM_001375611.1:c.973C>G	NP_001362540.1:p.Leu325Val
NM_001375613.1:c.973C>G	NP_001362542.1:p.Leu325Val