Canonical Allele Identifier: CA1723631119

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530822_87530862delinsCAAGAAAGCAAGAAAGCAAGAAAGAAAGAAAGAAAGAAAGA , CM000669.2:g.87530822_87530862delinsCAAGAAAGCAAGAAAGCAAGAAAGAAAGAAAGAAAGAAAGA	GRCh38
NC_000007.13:g.87160138_87160178delinsCAAGAAAGCAAGAAAGCAAGAAAGAAAGAAAGAAAGAAAGA , CM000669.1:g.87160138_87160178delinsCAAGAAAGCAAGAAAGCAAGAAAGAAAGAAAGAAAGAAAGA	GRCh37
NC_000007.12:g.86998074_86998114delinsCAAGAAAGCAAGAAAGCAAGAAAGAAAGAAAGAAAGAAAGA	NCBI36
NG_011513.1:g.187387_187427delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000265724.3:n.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTC...
ENST00000622132.5:c.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG MANE Select	ENSP00000478255.1:n.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTC...
ENST00000265724.7:c.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000265724.3:n.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTC...
ENST00000488737.6:n.327+432_327+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG
ENST00000496821.5:n.313+432_313+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG
ENST00000543898.5:c.2493+432_2493+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000444095.1:n.2493+432_2493+472delinsTCTTTCTTTCTTTCTTTC...
ENST00000622132.4:c.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000478255.1:n.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTC...
NM_000927.4:c.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_000918.2:n.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTT...
NM_001348944.1:c.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335873.1:n.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTT...
NM_001348945.1:c.2895+432_2895+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335874.1:n.2895+432_2895+472delinsTCTTTCTTTCTTTCTTTCTTT...
NM_001348946.1:c.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335875.1:n.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTT...
NM_001348946.2:c.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG MANE Select	NP_001335875.1:n.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTT...
NM_000927.5:c.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_000918.2:n.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTT...
NM_001348944.2:c.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335873.1:n.2685+432_2685+472delinsTCTTTCTTTCTTTCTTTCTTT...
NM_001348945.2:c.2895+432_2895+472delinsTCTTTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335874.1:n.2895+432_2895+472delinsTCTTTCTTTCTTTCTTTCTTT...