Canonical Allele Identifier: CA1723626761

Gene: ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87516598C= , CM000669.2:g.87516598C=	GRCh38
NC_000007.13:g.87145914C= , CM000669.1:g.87145914C=	GRCh37
NC_000007.12:g.86983850C=	NCBI36
NG_011513.1:g.201651G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001348946.2:c.2995G= MANE Select	NP_001335875.1:p.Ala999=
ENST00000622132.5:c.2995G= MANE Select	ENSP00000478255.1:p.Ala999=
NM_000927.4:c.2995G=	NP_000918.2:p.Ala999=
NM_000927.5:c.2995G=	NP_000918.2:p.Ala999=
NM_001348944.1:c.2995G=	NP_001335873.1:p.Ala999=
NM_001348944.2:c.2995G=	NP_001335873.1:p.Ala999=
NM_001348945.1:c.3205G=	NP_001335874.1:p.Ala1069=
NM_001348945.2:c.3205G=	NP_001335874.1:p.Ala1069=
NM_001348946.1:c.2995G=	NP_001335875.1:p.Ala999=
ENST00000265724.7:c.2995G=	ENSP00000265724.3:p.Ala999=
ENST00000265724.8:c.2995G=	ENSP00000265724.3:p.Ala999=
ENST00000475929.5:n.151G=
ENST00000483831.1:n.553G=
ENST00000488737.6:n.637G=
ENST00000496821.5:n.623G=
ENST00000543898.5:c.2803G=	ENSP00000444095.1:p.Ala935=
ENST00000622132.4:c.2995G=	ENSP00000478255.1:p.Ala999=