Canonical Allele Identifier: CA1104125864
Gene: ABCB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530803_87530804insCGCAAGAAAGGAAGAA , CM000669.2:g.87530803_87530804insCGCAAGAAAGGAAGAA GRCh38
NC_000007.13:g.87160119_87160120insCGCAAGAAAGGAAGAA , CM000669.1:g.87160119_87160120insCGCAAGAAAGGAAGAA GRCh37
NC_000007.12:g.86998055_86998056insCGCAAGAAAGGAAGAA NCBI36
NG_011513.1:g.187450_187451insCCTTTCTTGCGTTCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+495_2685+496insCCTTTCTTGCGTTCTT ENSP00000265724.3:n.2685+495_2685+496insCCTTTCTTGCGTTCTT
ENST00000622132.5:c.2685+495_2685+496insCCTTTCTTGCGTTCTT MANE Select ENSP00000478255.1:n.2685+495_2685+496insCCTTTCTTGCGTTCTT
ENST00000265724.7:c.2685+495_2685+496insCCTTTCTTGCGTTCTT ENSP00000265724.3:n.2685+495_2685+496insCCTTTCTTGCGTTCTT
ENST00000488737.6:n.327+495_327+496insCCTTTCTTGCGTTCTT
ENST00000496821.5:n.313+495_313+496insCCTTTCTTGCGTTCTT
ENST00000543898.5:c.2493+495_2493+496insCCTTTCTTGCGTTCTT ENSP00000444095.1:n.2493+495_2493+496insCCTTTCTTGCGTTCTT
ENST00000622132.4:c.2685+495_2685+496insCCTTTCTTGCGTTCTT ENSP00000478255.1:n.2685+495_2685+496insCCTTTCTTGCGTTCTT
NM_000927.4:c.2685+495_2685+496insCCTTTCTTGCGTTCTT NP_000918.2:n.2685+495_2685+496insCCTTTCTTGCGTTCTT
NM_001348944.1:c.2685+495_2685+496insCCTTTCTTGCGTTCTT NP_001335873.1:n.2685+495_2685+496insCCTTTCTTGCGTTCTT
NM_001348945.1:c.2895+495_2895+496insCCTTTCTTGCGTTCTT NP_001335874.1:n.2895+495_2895+496insCCTTTCTTGCGTTCTT
NM_001348946.1:c.2685+495_2685+496insCCTTTCTTGCGTTCTT NP_001335875.1:n.2685+495_2685+496insCCTTTCTTGCGTTCTT
NM_001348946.2:c.2685+495_2685+496insCCTTTCTTGCGTTCTT MANE Select NP_001335875.1:n.2685+495_2685+496insCCTTTCTTGCGTTCTT
NM_000927.5:c.2685+495_2685+496insCCTTTCTTGCGTTCTT NP_000918.2:n.2685+495_2685+496insCCTTTCTTGCGTTCTT
NM_001348944.2:c.2685+495_2685+496insCCTTTCTTGCGTTCTT NP_001335873.1:n.2685+495_2685+496insCCTTTCTTGCGTTCTT
NM_001348945.2:c.2895+495_2895+496insCCTTTCTTGCGTTCTT NP_001335874.1:n.2895+495_2895+496insCCTTTCTTGCGTTCTT