Canonical Allele Identifier: CA1104126228

Gene: ABCB1

Linked Data

• dbSNP Id: rs1816024197
• gnomAD v3: 7-87530882-G-GAAAAGA
• gnomAD v4: 7-87530882-G-GAAAAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530886_87530887insGAAAAA , CM000669.2:g.87530886_87530887insGAAAAA	GRCh38
NC_000007.13:g.87160202_87160203insGAAAAA , CM000669.1:g.87160202_87160203insGAAAAA	GRCh37
NC_000007.12:g.86998138_86998139insGAAAAA	NCBI36
NG_011513.1:g.187366_187367insTCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+411_2685+412insTCTTTT	ENSP00000265724.3:n.2685+411_2685+412insTCTTTT
ENST00000622132.5:c.2685+411_2685+412insTCTTTT MANE Select	ENSP00000478255.1:n.2685+411_2685+412insTCTTTT
ENST00000265724.7:c.2685+411_2685+412insTCTTTT	ENSP00000265724.3:n.2685+411_2685+412insTCTTTT
ENST00000488737.6:n.327+411_327+412insTCTTTT
ENST00000496821.5:n.313+411_313+412insTCTTTT
ENST00000543898.5:c.2493+411_2493+412insTCTTTT	ENSP00000444095.1:n.2493+411_2493+412insTCTTTT
ENST00000622132.4:c.2685+411_2685+412insTCTTTT	ENSP00000478255.1:n.2685+411_2685+412insTCTTTT
NM_000927.4:c.2685+411_2685+412insTCTTTT	NP_000918.2:n.2685+411_2685+412insTCTTTT
NM_001348944.1:c.2685+411_2685+412insTCTTTT	NP_001335873.1:n.2685+411_2685+412insTCTTTT
NM_001348945.1:c.2895+411_2895+412insTCTTTT	NP_001335874.1:n.2895+411_2895+412insTCTTTT
NM_001348946.1:c.2685+411_2685+412insTCTTTT	NP_001335875.1:n.2685+411_2685+412insTCTTTT
NM_001348946.2:c.2685+411_2685+412insTCTTTT MANE Select	NP_001335875.1:n.2685+411_2685+412insTCTTTT
NM_000927.5:c.2685+411_2685+412insTCTTTT	NP_000918.2:n.2685+411_2685+412insTCTTTT
NM_001348944.2:c.2685+411_2685+412insTCTTTT	NP_001335873.1:n.2685+411_2685+412insTCTTTT
NM_001348945.2:c.2895+411_2895+412insTCTTTT	NP_001335874.1:n.2895+411_2895+412insTCTTTT