Canonical Allele Identifier: CA1723646283

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87544763_87544764delinsCA , CM000669.2:g.87544763_87544764delinsCA	GRCh38
NC_000007.13:g.87174079_87174080delinsCA , CM000669.1:g.87174079_87174080delinsCA	GRCh37
NC_000007.12:g.87012015_87012016delinsCA	NCBI36
NG_011513.1:g.173485_173486delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2064+59_2064+60delinsTG	ENSP00000265724.3:n.2064+59_2064+60delinsTG
ENST00000622132.5:c.2064+59_2064+60delinsTG MANE Select	ENSP00000478255.1:n.2064+59_2064+60delinsTG
ENST00000265724.7:c.2064+59_2064+60delinsTG	ENSP00000265724.3:n.2064+59_2064+60delinsTG
ENST00000543898.5:c.1872+59_1872+60delinsTG	ENSP00000444095.1:n.1872+59_1872+60delinsTG
ENST00000622132.4:c.2064+59_2064+60delinsTG	ENSP00000478255.1:n.2064+59_2064+60delinsTG
NM_000927.4:c.2064+59_2064+60delinsTG	NP_000918.2:n.2064+59_2064+60delinsTG
NM_001348944.1:c.2064+59_2064+60delinsTG	NP_001335873.1:n.2064+59_2064+60delinsTG
NM_001348945.1:c.2274+59_2274+60delinsTG	NP_001335874.1:n.2274+59_2274+60delinsTG
NM_001348946.1:c.2064+59_2064+60delinsTG	NP_001335875.1:n.2064+59_2064+60delinsTG
NM_001348946.2:c.2064+59_2064+60delinsTG MANE Select	NP_001335875.1:n.2064+59_2064+60delinsTG
NM_000927.5:c.2064+59_2064+60delinsTG	NP_000918.2:n.2064+59_2064+60delinsTG
NM_001348944.2:c.2064+59_2064+60delinsTG	NP_001335873.1:n.2064+59_2064+60delinsTG
NM_001348945.2:c.2274+59_2274+60delinsTG	NP_001335874.1:n.2274+59_2274+60delinsTG