Canonical Allele Identifier: CA1723628485
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87520422_87520423delinsTC , CM000669.2:g.87520422_87520423delinsTC GRCh38
NC_000007.13:g.87149738_87149739delinsTC , CM000669.1:g.87149738_87149739delinsTC GRCh37
NC_000007.12:g.86987674_86987675delinsTC NCBI36
NG_011513.1:g.197826_197827delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000265724.8:c.2786+353_2786+354delinsGA ENSP00000265724.3:n.2786+353_2786+354deli...
ENST00000622132.5:c.2786+353_2786+354delinsGA MANE Select ENSP00000478255.1:n.2786+353_2786+354deli...
ENST00000265724.7:c.2786+353_2786+354delinsGA ENSP00000265724.3:n.2786+353_2786+354deli...
ENST00000483831.1:n.344+353_344+354delinsGA
ENST00000488737.6:n.428+353_428+354delinsGA
ENST00000496821.5:n.414+353_414+354delinsGA
ENST00000543898.5:c.2594+353_2594+354delinsGA ENSP00000444095.1:n.2594+353_2594+354deli...
ENST00000622132.4:c.2786+353_2786+354delinsGA ENSP00000478255.1:n.2786+353_2786+354deli...
NM_000927.4:c.2786+353_2786+354delinsGA NP_000918.2:n.2786+353_2786+354delinsGA
NM_001348944.1:c.2786+353_2786+354delinsGA NP_001335873.1:n.2786+353_2786+354delinsG...
NM_001348945.1:c.2996+353_2996+354delinsGA NP_001335874.1:n.2996+353_2996+354delinsG...
NM_001348946.1:c.2786+353_2786+354delinsGA NP_001335875.1:n.2786+353_2786+354delinsG...
NM_001348946.2:c.2786+353_2786+354delinsGA MANE Select NP_001335875.1:n.2786+353_2786+354delinsG...
NM_000927.5:c.2786+353_2786+354delinsGA NP_000918.2:n.2786+353_2786+354delinsGA
NM_001348944.2:c.2786+353_2786+354delinsGA NP_001335873.1:n.2786+353_2786+354delinsG...
NM_001348945.2:c.2996+353_2996+354delinsGA NP_001335874.1:n.2996+353_2996+354delinsG...