Canonical Allele Identifier: CA1723587091
Gene: ABCB4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87402185T= , CM000669.2:g.87402185T= GRCh38
NC_000007.13:g.87031501T= , CM000669.1:g.87031501T= GRCh37
NC_000007.12:g.86869437T= NCBI36
NG_007118.1:g.83248A=
NG_007118.2:g.83248A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359206.8:c.3751A= ENSP00000352135.3:p.Lys1251=
ENST00000649586.2:c.3751A= MANE Select ENSP00000496956.2:p.Lys1251=
ENST00000265723.8:c.3772A= ENSP00000265723.4:p.Lys1258=
ENST00000358400.7:c.3610A= ENSP00000351172.3:p.Lys1204=
ENST00000359206.7:c.3751A= ENSP00000352135.3:p.Lys1251=
ENST00000440025.1:c.185A=
ENST00000453593.5:c.3610A= ENSP00000392983.1:p.Lys1204=
ENST00000467983.1:n.363A=
NM_000443.3:c.3751A= NP_000434.1:p.Lys1251=
NM_018849.2:c.3772A= NP_061337.1:p.Lys1258=
NM_018850.2:c.3610A= NP_061338.1:p.Lys1204=
XM_011516308.1:c.3772A= XP_011514610.1:p.Lys1258=
XM_011516309.1:c.3751A= XP_011514611.1:p.Lys1251=
XM_011516310.1:c.3667A= XP_011514612.1:p.Lys1223=
XM_011516311.1:c.3643A= XP_011514613.1:p.Lys1215=
XM_011516312.1:c.3631A= XP_011514614.1:p.Lys1211=
XM_011516313.1:c.3610A= XP_011514615.1:p.Lys1204=
XM_011516314.1:c.3793A= XP_011514616.1:p.Lys1265=
XM_011516315.1:c.3112A= XP_011514617.1:p.Lys1038=
XM_011516308.3:c.4042A= XP_011514610.3:p.Lys1348=
XM_011516309.3:c.4021A= XP_011514611.3:p.Lys1341=
XM_011516310.3:c.3937A= XP_011514612.3:p.Lys1313=
XM_011516311.3:c.3913A= XP_011514613.3:p.Lys1305=
XM_011516312.3:c.3901A= XP_011514614.3:p.Lys1301=
XM_011516313.3:c.3880A= XP_011514615.2:p.Lys1294=
XM_011516315.3:c.3112A= XP_011514617.2:p.Lys1038=
XM_017012323.2:c.3772A= XP_016867812.1:p.Lys1258=
XR_001744809.2:n.4280A=
NM_000443.4:c.3751A= MANE Select NP_000434.1:p.Lys1251=
NM_018849.3:c.3772A= NP_061337.1:p.Lys1258=
NM_018850.3:c.3610A= NP_061338.1:p.Lys1204=