Canonical Allele Identifier: CA1723631071

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530814_87530846delinsCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGA , CM000669.2:g.87530814_87530846delinsCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGA	GRCh38
NC_000007.13:g.87160130_87160162delinsCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGA , CM000669.1:g.87160130_87160162delinsCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGA	GRCh37
NC_000007.12:g.86998066_86998098delinsCAAGAAAGCAAGAAAGCAAGAAAGCAAGAAAGA	NCBI36
NG_011513.1:g.187403_187435delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000265724.3:n.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGC...
ENST00000622132.5:c.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG MANE Select	ENSP00000478255.1:n.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGC...
ENST00000265724.7:c.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000265724.3:n.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGC...
ENST00000488737.6:n.327+448_327+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG
ENST00000496821.5:n.313+448_313+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG
ENST00000543898.5:c.2493+448_2493+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000444095.1:n.2493+448_2493+480delinsTCTTTCTTGCTTTCTTGC...
ENST00000622132.4:c.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000478255.1:n.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGC...
NM_000927.4:c.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_000918.2:n.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTT...
NM_001348944.1:c.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335873.1:n.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTT...
NM_001348945.1:c.2895+448_2895+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335874.1:n.2895+448_2895+480delinsTCTTTCTTGCTTTCTTGCTTT...
NM_001348946.1:c.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335875.1:n.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTT...
NM_001348946.2:c.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG MANE Select	NP_001335875.1:n.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTT...
NM_000927.5:c.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_000918.2:n.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTT...
NM_001348944.2:c.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335873.1:n.2685+448_2685+480delinsTCTTTCTTGCTTTCTTGCTTT...
NM_001348945.2:c.2895+448_2895+480delinsTCTTTCTTGCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335874.1:n.2895+448_2895+480delinsTCTTTCTTGCTTTCTTGCTTT...