Canonical Allele Identifier: CA575861944

Gene: ABCB1

Linked Data

• gnomAD v2: 7-87160149-G-GA
• MyVariant Identifiers: chr7:g.87160149_87160150insA (hg19) ; chr7:g.87530833_87530834insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87530836dup , CM000669.2:g.87530836dup	GRCh38
NC_000007.13:g.87160152dup , CM000669.1:g.87160152dup	GRCh37
NC_000007.12:g.86998088dup	NCBI36
NG_011513.1:g.187415dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265724.8:c.2685+460dup	ENSP00000265724.3:n.2685+460dup
ENST00000622132.5:c.2685+460dup MANE Select	ENSP00000478255.1:n.2685+460dup
ENST00000265724.7:c.2685+460dup	ENSP00000265724.3:n.2685+460dup
ENST00000488737.6:n.327+460dup
ENST00000496821.5:n.313+460dup
ENST00000543898.5:c.2493+460dup	ENSP00000444095.1:n.2493+460dup
ENST00000622132.4:c.2685+460dup	ENSP00000478255.1:n.2685+460dup
NM_000927.4:c.2685+460dup	NP_000918.2:n.2685+460dup
NM_001348944.1:c.2685+460dup	NP_001335873.1:n.2685+460dup
NM_001348945.1:c.2895+460dup	NP_001335874.1:n.2895+460dup
NM_001348946.1:c.2685+460dup	NP_001335875.1:n.2685+460dup
NM_001348946.2:c.2685+460dup MANE Select	NP_001335875.1:n.2685+460dup
NM_000927.5:c.2685+460dup	NP_000918.2:n.2685+460dup
NM_001348944.2:c.2685+460dup	NP_001335873.1:n.2685+460dup
NM_001348945.2:c.2895+460dup	NP_001335874.1:n.2895+460dup