Canonical Allele Identifier: CA388400294
Gene: ABCC4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.95170601C>A , CM000675.2:g.95170601C>A GRCh38
NC_000013.10:g.95822855C>A , CM000675.1:g.95822855C>A GRCh37
NC_000013.9:g.94620856C>A NCBI36
NG_050651.1:g.135846G>T
NG_050651.2:g.135846G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642524.1:c.*1788G>T ENSP00000493766.1:n.*1788G>T
ENST00000643051.1:c.1755G>T ENSP00000495513.1:p.Lys585Asn
ENST00000643556.1:c.1896G>T ENSP00000494938.1:n.1896G>T
ENST00000643816.1:n.2038G>T
ENST00000643842.1:c.*1801G>T ENSP00000493861.1:n.*1801G>T
ENST00000644471.1:n.1846G>T
ENST00000645237.2:c.1755G>T MANE Select ENSP00000494609.1:p.Lys585Asn
ENST00000645532.1:c.1794G>T ENSP00000494431.1:p.Lys598Asn
ENST00000646439.1:c.1755G>T ENSP00000494751.1:p.Lys585Asn
ENST00000376887.8:c.1755G>T ENSP00000366084.4:p.Lys585Asn
ENST00000536256.3:c.1530G>T ENSP00000442024.1:p.Lys510Asn
ENST00000629385.1:c.1755G>T ENSP00000487081.1:p.Lys585Asn
NM_001105515.2:c.1755G>T NP_001098985.1:p.Lys585Asn
NM_001301829.1:c.1755G>T NP_001288758.1:p.Lys585Asn
NM_001301830.1:c.1530G>T NP_001288759.1:p.Lys510Asn
NM_005845.4:c.1755G>T NP_005836.2:p.Lys585Asn
XM_005254025.2:c.1626G>T XP_005254082.1:p.Lys542Asn
XM_006719914.1:c.1665G>T XP_006719977.1:p.Lys555Asn
XM_011521047.1:c.1206G>T XP_011519349.1:p.Lys402Asn
XM_017020319.1:c.1626G>T XP_016875808.1:p.Lys542Asn
XM_017020320.2:c.1755G>T XP_016875809.1:p.Lys585Asn
XM_017020321.1:c.240G>T XP_016875810.1:p.Lys80Asn
XM_017020322.1:c.1626G>T XP_016875811.1:p.Lys542Asn
NM_001105515.3:c.1755G>T NP_001098985.1:p.Lys585Asn
NM_001301829.2:c.1755G>T NP_001288758.1:p.Lys585Asn
NM_001301830.2:c.1530G>T NP_001288759.1:p.Lys510Asn
NM_005845.5:c.1755G>T MANE Select NP_005836.2:p.Lys585Asn