Canonical Allele Identifier: CA2776825844
Gene: ABCB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87530847_87530848insGAAAGAAAGAAAGAAAGAC , CM000669.2:g.87530847_87530848insGAAAGAAAGAAAGAAAGAC GRCh38
NC_000007.13:g.87160163_87160164insGAAAGAAAGAAAGAAAGAC , CM000669.1:g.87160163_87160164insGAAAGAAAGAAAGAAAGAC GRCh37
NC_000007.12:g.86998099_86998100insGAAAGAAAGAAAGAAAGAC NCBI36
NG_011513.1:g.187401_187402insGTCTTTCTTTCTTTCTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC ENSP00000265724.3:n.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC
ENST00000622132.5:c.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC MANE Select ENSP00000478255.1:n.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC
ENST00000265724.7:c.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC ENSP00000265724.3:n.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC
ENST00000488737.6:n.327+446_327+447insGTCTTTCTTTCTTTCTTTC
ENST00000496821.5:n.313+446_313+447insGTCTTTCTTTCTTTCTTTC
ENST00000543898.5:c.2493+446_2493+447insGTCTTTCTTTCTTTCTTTC ENSP00000444095.1:n.2493+446_2493+447insGTCTTTCTTTCTTTCTTTC
ENST00000622132.4:c.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC ENSP00000478255.1:n.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC
NM_000927.4:c.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC NP_000918.2:n.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC
NM_001348944.1:c.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC NP_001335873.1:n.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC
NM_001348945.1:c.2895+446_2895+447insGTCTTTCTTTCTTTCTTTC NP_001335874.1:n.2895+446_2895+447insGTCTTTCTTTCTTTCTTTC
NM_001348946.1:c.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC NP_001335875.1:n.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC
NM_001348946.2:c.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC MANE Select NP_001335875.1:n.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC
NM_000927.5:c.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC NP_000918.2:n.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC
NM_001348944.2:c.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC NP_001335873.1:n.2685+446_2685+447insGTCTTTCTTTCTTTCTTTC
NM_001348945.2:c.2895+446_2895+447insGTCTTTCTTTCTTTCTTTC NP_001335874.1:n.2895+446_2895+447insGTCTTTCTTTCTTTCTTTC