Canonical Allele Identifier: CA348406478

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186395T>G (hg19) ; chr2:g.127428819T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428819T>G , CM000664.2:g.127428819T>G	GRCh38
NC_000002.11:g.128186395T>G , CM000664.1:g.128186395T>G	GRCh37
NC_000002.10:g.127902865T>G	NCBI36
NG_016323.1:g.15400T>G , LRG_599:g.15400T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1259T>G MANE Select	ENSP00000234071.4:p.Val420Gly
ENST00000234071.7:c.1259T>G	ENSP00000234071.3:p.Val420Gly
ENST00000402125.2:c.583T>G
ENST00000409048.1:c.1361T>G	ENSP00000386679.1:p.Val454Gly
NM_000312.3:c.1259T>G , LRG_599t1:c.1259T>G	NP_000303.1:p.Val420Gly
XM_005263715.3:c.1442T>G	XP_005263772.1:p.Val481Gly
XM_005263716.3:c.1424T>G	XP_005263773.1:p.Val475Gly
XM_005263717.3:c.1322T>G	XP_005263774.1:p.Val441Gly
XR_923313.1:n.1332-555A>C
XM_005263717.4:c.1322T>G	XP_005263774.1:p.Val441Gly
XM_017004505.1:c.1502T>G	XP_016859994.1:p.Val501Gly
XM_024453002.1:c.1604T>G	XP_024308770.1:p.Val535Gly
XM_024453003.1:c.1544T>G	XP_024308771.1:p.Val515Gly
XM_024453004.1:c.1442T>G	XP_024308772.1:p.Val481Gly
XM_024453005.1:c.1424T>G	XP_024308773.1:p.Val475Gly
XM_024453006.1:c.1361T>G	XP_024308774.1:p.Val454Gly
XR_001739705.1:n.3607-555A>C
XR_923313.2:n.4043-555A>C
NM_000312.4:c.1259T>G MANE Select	NP_000303.1:p.Val420Gly
NM_001375602.1:c.1442T>G	NP_001362531.1:p.Val481Gly
NM_001375603.1:c.1424T>G	NP_001362532.1:p.Val475Gly
NM_001375604.1:c.1322T>G	NP_001362533.1:p.Val441Gly
NM_001375605.1:c.1361T>G	NP_001362534.1:p.Val454Gly
NM_001375606.1:c.1427T>G	NP_001362535.1:p.Val476Gly
NM_001375607.1:c.1445T>G	NP_001362536.1:p.Val482Gly
NM_001375608.1:c.1202T>G	NP_001362537.1:p.Val401Gly
NM_001375609.1:c.1235T>G	NP_001362538.1:p.Val412Gly
NM_001375610.1:c.1253T>G	NP_001362539.1:p.Val418Gly
NM_001375611.1:c.1259T>G	NP_001362540.1:p.Val420Gly
NM_001375613.1:c.1259T>G	NP_001362542.1:p.Val420Gly