Canonical Allele Identifier: CA388402826
Community Standard Title: NM_005845.5(ABCC4):c.1460G>C (p.Gly487Ala)
Gene: ABCC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.95186786C>G , CM000675.2:g.95186786C>G GRCh38
NC_000013.10:g.95839040C>G , CM000675.1:g.95839040C>G GRCh37
NC_000013.9:g.94637041C>G NCBI36
NG_050651.1:g.119661G>C
NG_050651.2:g.119661G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005845.5:c.1460G>C MANE Select NP_005836.2:p.Gly487Ala
ENST00000645237.2:c.1460G>C MANE Select ENSP00000494609.1:p.Gly487Ala
NM_001105515.2:c.1460G>C NP_001098985.1:p.Gly487Ala
NM_001105515.3:c.1460G>C NP_001098985.1:p.Gly487Ala
NM_001301829.1:c.1460G>C NP_001288758.1:p.Gly487Ala
NM_001301829.2:c.1460G>C NP_001288758.1:p.Gly487Ala
NM_001301830.1:c.1235G>C NP_001288759.1:p.Gly412Ala
NM_001301830.2:c.1235G>C NP_001288759.1:p.Gly412Ala
NM_005845.4:c.1460G>C NP_005836.2:p.Gly487Ala
ENST00000376887.8:c.1460G>C ENSP00000366084.4:p.Gly487Ala
ENST00000536256.3:c.1235G>C ENSP00000442024.1:p.Gly412Ala
ENST00000629385.1:c.1460G>C ENSP00000487081.1:p.Gly487Ala
ENST00000642524.1:c.*1493G>C ENSP00000493766.1:n.*1493G>C
ENST00000643051.1:c.1460G>C ENSP00000495513.1:p.Gly487Ala
ENST00000643556.1:c.1601G>C ENSP00000494938.1:n.1601G>C
ENST00000643816.1:n.1743G>C
ENST00000643842.1:c.*1506G>C ENSP00000493861.1:n.*1506G>C
ENST00000644471.1:n.1556G>C
ENST00000645532.1:c.1499G>C ENSP00000494431.1:p.Gly500Ala
ENST00000646439.1:c.1460G>C ENSP00000494751.1:p.Gly487Ala
XM_005254025.2:c.1331G>C XP_005254082.1:p.Gly444Ala
XM_006719914.1:c.1370G>C XP_006719977.1:p.Gly457Ala
XM_011521047.1:c.911G>C XP_011519349.1:p.Gly304Ala
XM_017020319.1:c.1331G>C XP_016875808.1:p.Gly444Ala
XM_017020320.2:c.1460G>C XP_016875809.1:p.Gly487Ala
XM_017020322.1:c.1331G>C XP_016875811.1:p.Gly444Ala