Canonical Allele Identifier: CA348404766

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186043C>G (hg19) ; chr2:g.127428467C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428467C>G , CM000664.2:g.127428467C>G	GRCh38
NC_000002.11:g.128186043C>G , CM000664.1:g.128186043C>G	GRCh37
NC_000002.10:g.127902513C>G	NCBI36
NG_016323.1:g.15048C>G , LRG_599:g.15048C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.907C>G MANE Select	ENSP00000234071.4:p.Leu303Val
ENST00000234071.7:c.907C>G	ENSP00000234071.3:p.Leu303Val
ENST00000402125.2:c.231C>G
ENST00000409048.1:c.1009C>G	ENSP00000386679.1:p.Leu337Val
NM_000312.3:c.907C>G , LRG_599t1:c.907C>G	NP_000303.1:p.Leu303Val
XM_005263715.3:c.1090C>G	XP_005263772.1:p.Leu364Val
XM_005263716.3:c.1072C>G	XP_005263773.1:p.Leu358Val
XM_005263717.3:c.970C>G	XP_005263774.1:p.Leu324Val
XR_923313.1:n.1332-203G>C
XM_005263717.4:c.970C>G	XP_005263774.1:p.Leu324Val
XM_017004505.1:c.1150C>G	XP_016859994.1:p.Leu384Val
XM_024453002.1:c.1252C>G	XP_024308770.1:p.Leu418Val
XM_024453003.1:c.1192C>G	XP_024308771.1:p.Leu398Val
XM_024453004.1:c.1090C>G	XP_024308772.1:p.Leu364Val
XM_024453005.1:c.1072C>G	XP_024308773.1:p.Leu358Val
XM_024453006.1:c.1009C>G	XP_024308774.1:p.Leu337Val
XR_001739705.1:n.3607-203G>C
XR_923313.2:n.4043-203G>C
NM_000312.4:c.907C>G MANE Select	NP_000303.1:p.Leu303Val
NM_001375602.1:c.1090C>G	NP_001362531.1:p.Leu364Val
NM_001375603.1:c.1072C>G	NP_001362532.1:p.Leu358Val
NM_001375604.1:c.970C>G	NP_001362533.1:p.Leu324Val
NM_001375605.1:c.1009C>G	NP_001362534.1:p.Leu337Val
NM_001375606.1:c.1075C>G	NP_001362535.1:p.Leu359Val
NM_001375607.1:c.1093C>G	NP_001362536.1:p.Leu365Val
NM_001375608.1:c.850C>G	NP_001362537.1:p.Leu284Val
NM_001375609.1:c.883C>G	NP_001362538.1:p.Leu295Val
NM_001375610.1:c.901C>G	NP_001362539.1:p.Leu301Val
NM_001375611.1:c.907C>G	NP_001362540.1:p.Leu303Val
NM_001375613.1:c.907C>G	NP_001362542.1:p.Leu303Val