Canonical Allele Identifier: CA1474633690
Gene: ABCG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88169549_88169551delinsGAA , CM000666.2:g.88169549_88169551delinsGAA GRCh38
NC_000004.11:g.89090701_89090703delinsGAA , CM000666.1:g.89090701_89090703delinsGAA GRCh37
NC_000004.10:g.89309725_89309727delinsGAA NCBI36
NG_032067.2:g.66772_66774delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000650821.1:c.-19-29537_-19-29535delinsTTC ENSP00000498246.1:n.-19-29537_-19-29535delinsTTC
ENST00000515655.5:c.-19-29537_-19-29535delinsTTC ENSP00000426917.1:n.-19-29537_-19-29535delinsTTC
NM_001257386.1:c.-19-29537_-19-29535delinsTTC NP_001244315.1:n.-19-29537_-19-29535delinsTTC
XM_005263355.2:c.-19-29537_-19-29535delinsTTC XP_005263412.1:n.-19-29537_-19-29535delinsTTC
XM_011532420.1:c.-19-29537_-19-29535delinsTTC XP_011530722.1:n.-19-29537_-19-29535delinsTTC
NM_001257386.2:c.-19-29537_-19-29535delinsTTC NP_001244315.1:n.-19-29537_-19-29535delinsTTC
NM_001348985.1:c.-19-29537_-19-29535delinsTTC NP_001335914.1:n.-19-29537_-19-29535delinsTTC
XM_005263355.4:c.-19-29537_-19-29535delinsTTC XP_005263412.1:n.-19-29537_-19-29535delinsTTC
XM_011532420.3:c.-19-29537_-19-29535delinsTTC XP_011530722.1:n.-19-29537_-19-29535delinsTTC