Canonical Allele Identifier: CA254210816
Gene: ABCC4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.95209611del , CM000675.2:g.95209611del GRCh38
NC_000013.10:g.95861865del , CM000675.1:g.95861865del GRCh37
NC_000013.9:g.94659866del NCBI36
NG_050651.1:g.96836del
NG_050651.2:g.96836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000642524.1:c.*655-14del ENSP00000493766.1:n.*655-14del
ENST00000643051.1:c.622-14del ENSP00000495513.1:n.622-14del
ENST00000643556.1:c.763-14del ENSP00000494938.1:n.763-14del
ENST00000643816.1:n.905-14del
ENST00000643842.1:c.*668-14del ENSP00000493861.1:n.*668-14del
ENST00000644471.1:n.718-14del
ENST00000645237.2:c.622-14del MANE Select ENSP00000494609.1:n.622-14del
ENST00000645532.1:c.661-14del ENSP00000494431.1:n.661-14del
ENST00000646439.1:c.622-14del ENSP00000494751.1:n.622-14del
ENST00000376887.8:c.622-14del ENSP00000366084.4:n.622-14del
ENST00000536256.3:c.397-14del ENSP00000442024.1:n.397-14del
ENST00000629385.1:c.622-14del ENSP00000487081.1:n.622-14del
NM_001105515.2:c.622-14del NP_001098985.1:n.622-14del
NM_001301829.1:c.622-14del NP_001288758.1:n.622-14del
NM_001301830.1:c.397-14del NP_001288759.1:n.397-14del
NM_005845.4:c.622-14del NP_005836.2:n.622-14del
XM_005254025.2:c.493-14del XP_005254082.1:n.493-14del
XM_006719914.1:c.622-14del XP_006719977.1:n.622-14del
XM_011521047.1:c.73-14del XP_011519349.1:n.73-14del
XM_017020319.1:c.493-14del XP_016875808.1:n.493-14del
XM_017020320.2:c.622-14del XP_016875809.1:n.622-14del
XM_017020322.1:c.493-14del XP_016875811.1:n.493-14del
NM_001105515.3:c.622-14del NP_001098985.1:n.622-14del
NM_001301829.2:c.622-14del NP_001288758.1:n.622-14del
NM_001301830.2:c.397-14del NP_001288759.1:n.397-14del
NM_005845.5:c.622-14del MANE Select NP_005836.2:n.622-14del
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