Canonical Allele Identifier: CA1474633800

Gene: ABCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88169788_88169789delinsAG , CM000666.2:g.88169788_88169789delinsAG	GRCh38
NC_000004.11:g.89090940_89090941delinsAG , CM000666.1:g.89090940_89090941delinsAG	GRCh37
NC_000004.10:g.89309964_89309965delinsAG	NCBI36
NG_032067.2:g.66534_66535delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000650821.1:c.-19-29775_-19-29774delinsCT	ENSP00000498246.1:n.-19-29775_-19-29774delinsCT
ENST00000515655.5:c.-19-29775_-19-29774delinsCT	ENSP00000426917.1:n.-19-29775_-19-29774delinsCT
NM_001257386.1:c.-19-29775_-19-29774delinsCT	NP_001244315.1:n.-19-29775_-19-29774delinsCT
XM_005263355.2:c.-19-29775_-19-29774delinsCT	XP_005263412.1:n.-19-29775_-19-29774delinsCT
XM_011532420.1:c.-19-29775_-19-29774delinsCT	XP_011530722.1:n.-19-29775_-19-29774delinsCT
NM_001257386.2:c.-19-29775_-19-29774delinsCT	NP_001244315.1:n.-19-29775_-19-29774delinsCT
NM_001348985.1:c.-19-29775_-19-29774delinsCT	NP_001335914.1:n.-19-29775_-19-29774delinsCT
XM_005263355.4:c.-19-29775_-19-29774delinsCT	XP_005263412.1:n.-19-29775_-19-29774delinsCT
XM_011532420.3:c.-19-29775_-19-29774delinsCT	XP_011530722.1:n.-19-29775_-19-29774delinsCT