Canonical Allele Identifier: CA2220718241
Gene: ABCC11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.48224303G= , CM000678.2:g.48224303G= GRCh38
NC_000016.9:g.48258214G= , CM000678.1:g.48258214G= GRCh37
NC_000016.8:g.46815715G= NCBI36
NG_011522.1:g.15875C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356608.7:c.522C= MANE Select ENSP00000349017.2:p.Cys174=
ENST00000353782.9:c.522C= ENSP00000311326.6:p.Cys174=
ENST00000356608.6:c.522C= ENSP00000349017.2:p.Cys174=
ENST00000394747.5:c.522C= ENSP00000378230.1:p.Cys174=
ENST00000394748.5:c.522C= ENSP00000378231.1:p.Cys174=
ENST00000567385.5:n.920C=
NM_032583.3:c.522C= NP_115972.2:p.Cys174=
NM_033151.3:c.522C= NP_149163.2:p.Cys174=
NM_145186.2:c.522C= NP_660187.1:p.Cys174=
XM_011523396.1:c.324C= XP_011521698.1:p.Cys108=
XM_017023795.2:c.522C= XP_016879284.1:p.Cys174=
XM_017023796.2:c.522C= XP_016879285.1:p.Cys174=
XM_017023797.2:c.522C= XP_016879286.1:p.Cys174=
XM_017023798.2:c.522C= XP_016879287.1:p.Cys174=
XM_017023799.2:c.522C= XP_016879288.1:p.Cys174=
XM_017023800.2:c.522C= XP_016879289.1:p.Cys174=
XM_017023801.2:c.522C= XP_016879290.1:p.Cys174=
XM_017023803.1:c.522C= XP_016879292.1:p.Cys174=
XR_001752012.1:n.3200C=
NM_001370496.1:c.522C= NP_001357425.1:p.Cys174=
NM_001370497.1:c.522C= MANE Select NP_001357426.1:p.Cys174=
NM_032583.4:c.522C= NP_115972.2:p.Cys174=
NM_033151.4:c.522C= NP_149163.2:p.Cys174=
NM_145186.3:c.522C= NP_660187.1:p.Cys174=