Canonical Allele Identifier: CA1723631645

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530903_87530907delinsGGGAA , CM000669.2:g.87530903_87530907delinsGGGAA	GRCh38
NC_000007.13:g.87160219_87160223delinsGGGAA , CM000669.1:g.87160219_87160223delinsGGGAA	GRCh37
NC_000007.12:g.86998155_86998159delinsGGGAA	NCBI36
NG_011513.1:g.187342_187346delinsTTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+387_2685+391delinsTTCCC	ENSP00000265724.3:n.2685+387_2685+391delinsTTCCC
ENST00000622132.5:c.2685+387_2685+391delinsTTCCC MANE Select	ENSP00000478255.1:n.2685+387_2685+391delinsTTCCC
ENST00000265724.7:c.2685+387_2685+391delinsTTCCC	ENSP00000265724.3:n.2685+387_2685+391delinsTTCCC
ENST00000488737.6:n.327+387_327+391delinsTTCCC
ENST00000496821.5:n.313+387_313+391delinsTTCCC
ENST00000543898.5:c.2493+387_2493+391delinsTTCCC	ENSP00000444095.1:n.2493+387_2493+391delinsTTCCC
ENST00000622132.4:c.2685+387_2685+391delinsTTCCC	ENSP00000478255.1:n.2685+387_2685+391delinsTTCCC
NM_000927.4:c.2685+387_2685+391delinsTTCCC	NP_000918.2:n.2685+387_2685+391delinsTTCCC
NM_001348944.1:c.2685+387_2685+391delinsTTCCC	NP_001335873.1:n.2685+387_2685+391delinsTTCCC
NM_001348945.1:c.2895+387_2895+391delinsTTCCC	NP_001335874.1:n.2895+387_2895+391delinsTTCCC
NM_001348946.1:c.2685+387_2685+391delinsTTCCC	NP_001335875.1:n.2685+387_2685+391delinsTTCCC
NM_001348946.2:c.2685+387_2685+391delinsTTCCC MANE Select	NP_001335875.1:n.2685+387_2685+391delinsTTCCC
NM_000927.5:c.2685+387_2685+391delinsTTCCC	NP_000918.2:n.2685+387_2685+391delinsTTCCC
NM_001348944.2:c.2685+387_2685+391delinsTTCCC	NP_001335873.1:n.2685+387_2685+391delinsTTCCC
NM_001348945.2:c.2895+387_2895+391delinsTTCCC	NP_001335874.1:n.2895+387_2895+391delinsTTCCC