Canonical Allele Identifier: CA1723626317
Gene: ABCB1 HGNC NCBI

Linked Data

dbSNP Id: rs1815206877

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87515645_87515646insCA , CM000669.2:g.87515645_87515646insCA GRCh38
NC_000007.13:g.87144961_87144962insCA , CM000669.1:g.87144961_87144962insCA GRCh37
NC_000007.12:g.86982897_86982898insCA NCBI36
NG_011513.1:g.202603_202604insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265724.8:c.3085-218_3085-217insTG ENSP00000265724.3:n.3085-218_3085-217insTG
ENST00000622132.5:c.3085-218_3085-217insTG MANE Select ENSP00000478255.1:n.3085-218_3085-217insTG
ENST00000265724.7:c.3085-218_3085-217insTG ENSP00000265724.3:n.3085-218_3085-217insTG
ENST00000475929.5:n.241-218_241-217insTG
ENST00000488737.6:n.727-218_727-217insTG
ENST00000496821.5:n.713-218_713-217insTG
ENST00000543898.5:c.2893-218_2893-217insTG ENSP00000444095.1:n.2893-218_2893-217insTG
ENST00000622132.4:c.3085-218_3085-217insTG ENSP00000478255.1:n.3085-218_3085-217insTG
NM_000927.4:c.3085-218_3085-217insTG NP_000918.2:n.3085-218_3085-217insTG
NM_001348944.1:c.3085-218_3085-217insTG NP_001335873.1:n.3085-218_3085-217insTG
NM_001348945.1:c.3295-218_3295-217insTG NP_001335874.1:n.3295-218_3295-217insTG
NM_001348946.1:c.3085-218_3085-217insTG NP_001335875.1:n.3085-218_3085-217insTG
NM_001348946.2:c.3085-218_3085-217insTG MANE Select NP_001335875.1:n.3085-218_3085-217insTG
NM_000927.5:c.3085-218_3085-217insTG NP_000918.2:n.3085-218_3085-217insTG
NM_001348944.2:c.3085-218_3085-217insTG NP_001335873.1:n.3085-218_3085-217insTG
NM_001348945.2:c.3295-218_3295-217insTG NP_001335874.1:n.3295-218_3295-217insTG