Canonical Allele Identifier: CA1723593010

Gene: ABCB4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87431549_87431559delinsGTCCGGCCTTC , CM000669.2:g.87431549_87431559delinsGTCCGGCCTTC	GRCh38
NC_000007.13:g.87060865_87060875delinsGTCCGGCCTTC , CM000669.1:g.87060865_87060875delinsGTCCGGCCTTC	GRCh37
NC_000007.12:g.86898801_86898811delinsGTCCGGCCTTC	NCBI36
NG_007118.1:g.53874_53884delinsGAAGGCCGGAC
NG_007118.2:g.53874_53884delinsGAAGGCCGGAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000359206.8:c.1738_1748delinsGAAGGCCGGAC	ENSP00000352135.3:p.Glu580=
ENST00000643670.1:c.1754_1764delinsGAAGGCCGGAC	ENSP00000496629.1:n.1754_1764delinsGAAGGC...
ENST00000644106.1:c.*1275_*1285delinsGAAGGCCGGAC	ENSP00000493477.1:n.*1275_*1285delinsGAAG...
ENST00000649586.2:c.1738_1748delinsGAAGGCCGGAC MANE Select	ENSP00000496956.2:p.Glu580=
ENST00000265723.8:c.1738_1748delinsGAAGGCCGGAC	ENSP00000265723.4:p.Glu580=
ENST00000358400.7:c.1738_1748delinsGAAGGCCGGAC	ENSP00000351172.3:p.Glu580=
ENST00000359206.7:c.1738_1748delinsGAAGGCCGGAC	ENSP00000352135.3:p.Glu580=
ENST00000453593.5:c.1738_1748delinsGAAGGCCGGAC	ENSP00000392983.1:p.Glu580=
NM_000443.3:c.1738_1748delinsGAAGGCCGGAC	NP_000434.1:p.Glu580=
NM_018849.2:c.1738_1748delinsGAAGGCCGGAC	NP_061337.1:p.Glu580=
NM_018850.2:c.1738_1748delinsGAAGGCCGGAC	NP_061338.1:p.Glu580=
XM_011516308.1:c.1738_1748delinsGAAGGCCGGAC	XP_011514610.1:p.Glu580=
XM_011516309.1:c.1738_1748delinsGAAGGCCGGAC	XP_011514611.1:p.Glu580=
XM_011516310.1:c.1738_1748delinsGAAGGCCGGAC	XP_011514612.1:p.Glu580=
XM_011516311.1:c.1738_1748delinsGAAGGCCGGAC	XP_011514613.1:p.Glu580=
XM_011516312.1:c.1738_1748delinsGAAGGCCGGAC	XP_011514614.1:p.Glu580=
XM_011516313.1:c.1738_1748delinsGAAGGCCGGAC	XP_011514615.1:p.Glu580=
XM_011516314.1:c.1759_1769delinsGAAGGCCGGAC	XP_011514616.1:p.Glu587=
XM_011516315.1:c.1078_1088delinsGAAGGCCGGAC	XP_011514617.1:p.Glu360=
XR_927478.1:n.1834_1844delinsGAAGGCCGGAC
XM_011516308.3:c.2008_2018delinsGAAGGCCGGAC	XP_011514610.3:p.Glu670=
XM_011516309.3:c.2008_2018delinsGAAGGCCGGAC	XP_011514611.3:p.Glu670=
XM_011516310.3:c.2008_2018delinsGAAGGCCGGAC	XP_011514612.3:p.Glu670=
XM_011516311.3:c.2008_2018delinsGAAGGCCGGAC	XP_011514613.3:p.Glu670=
XM_011516312.3:c.2008_2018delinsGAAGGCCGGAC	XP_011514614.3:p.Glu670=
XM_011516313.3:c.2008_2018delinsGAAGGCCGGAC	XP_011514615.2:p.Glu670=
XM_011516315.3:c.1078_1088delinsGAAGGCCGGAC	XP_011514617.2:p.Glu360=
XM_017012323.2:c.1738_1748delinsGAAGGCCGGAC	XP_016867812.1:p.Glu580=
XR_001744809.2:n.2509_2519delinsGAAGGCCGGAC
XR_001744810.2:n.2504_2514delinsGAAGGCCGGAC
NM_000443.4:c.1738_1748delinsGAAGGCCGGAC MANE Select	NP_000434.1:p.Glu580=
NM_018849.3:c.1738_1748delinsGAAGGCCGGAC	NP_061337.1:p.Glu580=
NM_018850.3:c.1738_1748delinsGAAGGCCGGAC	NP_061338.1:p.Glu580=