Canonical Allele Identifier: CA1723631120

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530822_87530858delinsCAAGAAAGCAAGAAAGCAAGAAAGAAAGAAAGAAAGA , CM000669.2:g.87530822_87530858delinsCAAGAAAGCAAGAAAGCAAGAAAGAAAGAAAGAAAGA	GRCh38
NC_000007.13:g.87160138_87160174delinsCAAGAAAGCAAGAAAGCAAGAAAGAAAGAAAGAAAGA , CM000669.1:g.87160138_87160174delinsCAAGAAAGCAAGAAAGCAAGAAAGAAAGAAAGAAAGA	GRCh37
NC_000007.12:g.86998074_86998110delinsCAAGAAAGCAAGAAAGCAAGAAAGAAAGAAAGAAAGA	NCBI36
NG_011513.1:g.187391_187427delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000265724.3:n.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTC...
ENST00000622132.5:c.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG MANE Select	ENSP00000478255.1:n.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTC...
ENST00000265724.7:c.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000265724.3:n.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTC...
ENST00000488737.6:n.327+436_327+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG
ENST00000496821.5:n.313+436_313+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG
ENST00000543898.5:c.2493+436_2493+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000444095.1:n.2493+436_2493+472delinsTCTTTCTTTCTTTCTTTC...
ENST00000622132.4:c.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	ENSP00000478255.1:n.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTC...
NM_000927.4:c.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_000918.2:n.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTT...
NM_001348944.1:c.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335873.1:n.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTG...
NM_001348945.1:c.2895+436_2895+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335874.1:n.2895+436_2895+472delinsTCTTTCTTTCTTTCTTTCTTG...
NM_001348946.1:c.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335875.1:n.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTG...
NM_001348946.2:c.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG MANE Select	NP_001335875.1:n.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTG...
NM_000927.5:c.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_000918.2:n.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTT...
NM_001348944.2:c.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335873.1:n.2685+436_2685+472delinsTCTTTCTTTCTTTCTTTCTTG...
NM_001348945.2:c.2895+436_2895+472delinsTCTTTCTTTCTTTCTTTCTTGCTTTCTTGCTTTCTTG	NP_001335874.1:n.2895+436_2895+472delinsTCTTTCTTTCTTTCTTTCTTG...