Canonical Allele Identifier: CA1723630704
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87551491_87551492delinsAT , CM000669.2:g.87551491_87551492delinsAT GRCh38
NC_000007.13:g.87180807_87180808delinsAT , CM000669.1:g.87180807_87180808delinsAT GRCh37
NC_000007.12:g.87018743_87018744delinsAT NCBI36
NG_011513.1:g.166757_166758delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.1000-654_1000-653delinsAT ENSP00000265724.3:n.1000-654_1000-653delinsAT
ENST00000622132.5:c.1000-654_1000-653delinsAT MANE Select ENSP00000478255.1:n.1000-654_1000-653delinsAT
ENST00000265724.7:c.1000-654_1000-653delinsAT ENSP00000265724.3:n.1000-654_1000-653delinsAT
ENST00000543898.5:c.808-654_808-653delinsAT ENSP00000444095.1:n.808-654_808-653delinsAT
ENST00000622132.4:c.1000-654_1000-653delinsAT ENSP00000478255.1:n.1000-654_1000-653delinsAT
NM_000927.4:c.1000-654_1000-653delinsAT NP_000918.2:n.1000-654_1000-653delinsAT
NM_001348944.1:c.1000-654_1000-653delinsAT NP_001335873.1:n.1000-654_1000-653delinsAT
NM_001348945.1:c.1210-654_1210-653delinsAT NP_001335874.1:n.1210-654_1210-653delinsAT
NM_001348946.1:c.1000-654_1000-653delinsAT NP_001335875.1:n.1000-654_1000-653delinsAT
NM_001348946.2:c.1000-654_1000-653delinsAT MANE Select NP_001335875.1:n.1000-654_1000-653delinsAT
NM_000927.5:c.1000-654_1000-653delinsAT NP_000918.2:n.1000-654_1000-653delinsAT
NM_001348944.2:c.1000-654_1000-653delinsAT NP_001335873.1:n.1000-654_1000-653delinsAT
NM_001348945.2:c.1210-654_1210-653delinsAT NP_001335874.1:n.1210-654_1210-653delinsAT