Canonical Allele Identifier: CA913189581

Gene: ABCB4

Linked Data

• ClinVar Variation Id: 597519
• ClinVar RCV Id: RCV000733668
• dbSNP Id: rs1562975541

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87439750_87439763delinsCCTGAATGG , CM000669.2:g.87439750_87439763delinsCCTGAATGG	GRCh38
NC_000007.13:g.87069066_87069079delinsCCTGAATGG , CM000669.1:g.87069066_87069079delinsCCTGAATGG	GRCh37
NC_000007.12:g.86907002_86907015delinsCCTGAATGG	NCBI36
NG_007118.1:g.45670_45683delinsCCATTCAGG
NG_007118.2:g.45670_45683delinsCCATTCAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000359206.8:c.1635_1648delinsCCATTCAGG	ENSP00000352135.3:p.Ala546HisfsTer11
ENST00000643670.1:c.1651_1664delinsCCATTCAGG	ENSP00000496629.1:n.1651_1664delinsCCATTC...
ENST00000644106.1:c.*1172_*1185delinsCCATTCAGG	ENSP00000493477.1:n.*1172_*1185delinsCCAT...
ENST00000649586.2:c.1635_1648delinsCCATTCAGG MANE Select	ENSP00000496956.2:p.Ala546HisfsTer11
ENST00000265723.8:c.1635_1648delinsCCATTCAGG	ENSP00000265723.4:p.Ala546HisfsTer11
ENST00000358400.7:c.1635_1648delinsCCATTCAGG	ENSP00000351172.3:p.Ala546HisfsTer11
ENST00000359206.7:c.1635_1648delinsCCATTCAGG	ENSP00000352135.3:p.Ala546HisfsTer11
ENST00000453593.5:c.1635_1648delinsCCATTCAGG	ENSP00000392983.1:p.Ala546HisfsTer11
NM_000443.3:c.1635_1648delinsCCATTCAGG	NP_000434.1:p.Ala546HisfsTer11
NM_018849.2:c.1635_1648delinsCCATTCAGG	NP_061337.1:p.Ala546HisfsTer11
NM_018850.2:c.1635_1648delinsCCATTCAGG	NP_061338.1:p.Ala546HisfsTer11
XM_011516308.1:c.1635_1648delinsCCATTCAGG	XP_011514610.1:p.Ala546HisfsTer11
XM_011516309.1:c.1635_1648delinsCCATTCAGG	XP_011514611.1:p.Ala546HisfsTer11
XM_011516310.1:c.1635_1648delinsCCATTCAGG	XP_011514612.1:p.Ala546HisfsTer11
XM_011516311.1:c.1635_1648delinsCCATTCAGG	XP_011514613.1:p.Ala546HisfsTer11
XM_011516312.1:c.1635_1648delinsCCATTCAGG	XP_011514614.1:p.Ala546HisfsTer11
XM_011516313.1:c.1635_1648delinsCCATTCAGG	XP_011514615.1:p.Ala546HisfsTer11
XM_011516314.1:c.1656_1669delinsCCATTCAGG	XP_011514616.1:p.Ala553HisfsTer11
XM_011516315.1:c.975_988delinsCCATTCAGG	XP_011514617.1:p.Ala326HisfsTer11
XR_927478.1:n.1731_1744delinsCCATTCAGG
XM_011516308.3:c.1905_1918delinsCCATTCAGG	XP_011514610.3:p.Ala636HisfsTer11
XM_011516309.3:c.1905_1918delinsCCATTCAGG	XP_011514611.3:p.Ala636HisfsTer11
XM_011516310.3:c.1905_1918delinsCCATTCAGG	XP_011514612.3:p.Ala636HisfsTer11
XM_011516311.3:c.1905_1918delinsCCATTCAGG	XP_011514613.3:p.Ala636HisfsTer11
XM_011516312.3:c.1905_1918delinsCCATTCAGG	XP_011514614.3:p.Ala636HisfsTer11
XM_011516313.3:c.1905_1918delinsCCATTCAGG	XP_011514615.2:p.Ala636HisfsTer11
XM_011516315.3:c.975_988delinsCCATTCAGG	XP_011514617.2:p.Ala326HisfsTer11
XM_017012323.2:c.1635_1648delinsCCATTCAGG	XP_016867812.1:p.Ala546HisfsTer11
XR_001744809.2:n.2406_2419delinsCCATTCAGG
XR_001744810.2:n.2401_2414delinsCCATTCAGG
NM_000443.4:c.1635_1648delinsCCATTCAGG MANE Select	NP_000434.1:p.Ala546HisfsTer11
NM_018849.3:c.1635_1648delinsCCATTCAGG	NP_061337.1:p.Ala546HisfsTer11
NM_018850.3:c.1635_1648delinsCCATTCAGG	NP_061338.1:p.Ala546HisfsTer11