Canonical Allele Identifier: CA1723631654

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530909_87530917delinsGAAGGAAAA , CM000669.2:g.87530909_87530917delinsGAAGGAAAA	GRCh38
NC_000007.13:g.87160225_87160233delinsGAAGGAAAA , CM000669.1:g.87160225_87160233delinsGAAGGAAAA	GRCh37
NC_000007.12:g.86998161_86998169delinsGAAGGAAAA	NCBI36
NG_011513.1:g.187332_187340delinsTTTTCCTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+377_2685+385delinsTTTTCCTTC	ENSP00000265724.3:n.2685+377_2685+385delinsTTTTCCTTC
ENST00000622132.5:c.2685+377_2685+385delinsTTTTCCTTC MANE Select	ENSP00000478255.1:n.2685+377_2685+385delinsTTTTCCTTC
ENST00000265724.7:c.2685+377_2685+385delinsTTTTCCTTC	ENSP00000265724.3:n.2685+377_2685+385delinsTTTTCCTTC
ENST00000488737.6:n.327+377_327+385delinsTTTTCCTTC
ENST00000496821.5:n.313+377_313+385delinsTTTTCCTTC
ENST00000543898.5:c.2493+377_2493+385delinsTTTTCCTTC	ENSP00000444095.1:n.2493+377_2493+385delinsTTTTCCTTC
ENST00000622132.4:c.2685+377_2685+385delinsTTTTCCTTC	ENSP00000478255.1:n.2685+377_2685+385delinsTTTTCCTTC
NM_000927.4:c.2685+377_2685+385delinsTTTTCCTTC	NP_000918.2:n.2685+377_2685+385delinsTTTTCCTTC
NM_001348944.1:c.2685+377_2685+385delinsTTTTCCTTC	NP_001335873.1:n.2685+377_2685+385delinsTTTTCCTTC
NM_001348945.1:c.2895+377_2895+385delinsTTTTCCTTC	NP_001335874.1:n.2895+377_2895+385delinsTTTTCCTTC
NM_001348946.1:c.2685+377_2685+385delinsTTTTCCTTC	NP_001335875.1:n.2685+377_2685+385delinsTTTTCCTTC
NM_001348946.2:c.2685+377_2685+385delinsTTTTCCTTC MANE Select	NP_001335875.1:n.2685+377_2685+385delinsTTTTCCTTC
NM_000927.5:c.2685+377_2685+385delinsTTTTCCTTC	NP_000918.2:n.2685+377_2685+385delinsTTTTCCTTC
NM_001348944.2:c.2685+377_2685+385delinsTTTTCCTTC	NP_001335873.1:n.2685+377_2685+385delinsTTTTCCTTC
NM_001348945.2:c.2895+377_2895+385delinsTTTTCCTTC	NP_001335874.1:n.2895+377_2895+385delinsTTTTCCTTC