Canonical Allele Identifier: CA348405951

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186272A>G (hg19) ; chr2:g.127428696A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428696A>G , CM000664.2:g.127428696A>G	GRCh38
NC_000002.11:g.128186272A>G , CM000664.1:g.128186272A>G	GRCh37
NC_000002.10:g.127902742A>G	NCBI36
NG_016323.1:g.15277A>G , LRG_599:g.15277A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1136A>G MANE Select	ENSP00000234071.4:p.Asn379Ser
ENST00000234071.7:c.1136A>G	ENSP00000234071.3:p.Asn379Ser
ENST00000402125.2:c.460A>G
ENST00000409048.1:c.1238A>G	ENSP00000386679.1:p.Asn413Ser
NM_000312.3:c.1136A>G , LRG_599t1:c.1136A>G	NP_000303.1:p.Asn379Ser
XM_005263715.3:c.1319A>G	XP_005263772.1:p.Asn440Ser
XM_005263716.3:c.1301A>G	XP_005263773.1:p.Asn434Ser
XM_005263717.3:c.1199A>G	XP_005263774.1:p.Asn400Ser
XR_923313.1:n.1332-432T>C
XM_005263717.4:c.1199A>G	XP_005263774.1:p.Asn400Ser
XM_017004505.1:c.1379A>G	XP_016859994.1:p.Asn460Ser
XM_024453002.1:c.1481A>G	XP_024308770.1:p.Asn494Ser
XM_024453003.1:c.1421A>G	XP_024308771.1:p.Asn474Ser
XM_024453004.1:c.1319A>G	XP_024308772.1:p.Asn440Ser
XM_024453005.1:c.1301A>G	XP_024308773.1:p.Asn434Ser
XM_024453006.1:c.1238A>G	XP_024308774.1:p.Asn413Ser
XR_001739705.1:n.3607-432T>C
XR_923313.2:n.4043-432T>C
NM_000312.4:c.1136A>G MANE Select	NP_000303.1:p.Asn379Ser
NM_001375602.1:c.1319A>G	NP_001362531.1:p.Asn440Ser
NM_001375603.1:c.1301A>G	NP_001362532.1:p.Asn434Ser
NM_001375604.1:c.1199A>G	NP_001362533.1:p.Asn400Ser
NM_001375605.1:c.1238A>G	NP_001362534.1:p.Asn413Ser
NM_001375606.1:c.1304A>G	NP_001362535.1:p.Asn435Ser
NM_001375607.1:c.1322A>G	NP_001362536.1:p.Asn441Ser
NM_001375608.1:c.1079A>G	NP_001362537.1:p.Asn360Ser
NM_001375609.1:c.1112A>G	NP_001362538.1:p.Asn371Ser
NM_001375610.1:c.1130A>G	NP_001362539.1:p.Asn377Ser
NM_001375611.1:c.1136A>G	NP_001362540.1:p.Asn379Ser
NM_001375613.1:c.1136A>G	NP_001362542.1:p.Asn379Ser