Canonical Allele Identifier: CA395824741
Gene: ABCC11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.48224289A>G , CM000678.2:g.48224289A>G GRCh38
NC_000016.9:g.48258200A>G , CM000678.1:g.48258200A>G GRCh37
NC_000016.8:g.46815701A>G NCBI36
NG_011522.1:g.15889T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000356608.7:c.536T>C MANE Select ENSP00000349017.2:p.Leu179Pro
ENST00000353782.9:c.536T>C ENSP00000311326.6:p.Leu179Pro
ENST00000356608.6:c.536T>C ENSP00000349017.2:p.Leu179Pro
ENST00000394747.5:c.536T>C ENSP00000378230.1:p.Leu179Pro
ENST00000394748.5:c.536T>C ENSP00000378231.1:p.Leu179Pro
ENST00000567385.5:n.934T>C
NM_032583.3:c.536T>C NP_115972.2:p.Leu179Pro
NM_033151.3:c.536T>C NP_149163.2:p.Leu179Pro
NM_145186.2:c.536T>C NP_660187.1:p.Leu179Pro
XM_011523396.1:c.338T>C XP_011521698.1:p.Leu113Pro
XM_017023795.2:c.536T>C XP_016879284.1:p.Leu179Pro
XM_017023796.2:c.536T>C XP_016879285.1:p.Leu179Pro
XM_017023797.2:c.536T>C XP_016879286.1:p.Leu179Pro
XM_017023798.2:c.536T>C XP_016879287.1:p.Leu179Pro
XM_017023799.2:c.536T>C XP_016879288.1:p.Leu179Pro
XM_017023800.2:c.536T>C XP_016879289.1:p.Leu179Pro
XM_017023801.2:c.536T>C XP_016879290.1:p.Leu179Pro
XM_017023803.1:c.536T>C XP_016879292.1:p.Leu179Pro
XR_001752012.1:n.3214T>C
NM_001370496.1:c.536T>C NP_001357425.1:p.Leu179Pro
NM_001370497.1:c.536T>C MANE Select NP_001357426.1:p.Leu179Pro
NM_032583.4:c.536T>C NP_115972.2:p.Leu179Pro
NM_033151.4:c.536T>C NP_149163.2:p.Leu179Pro
NM_145186.3:c.536T>C NP_660187.1:p.Leu179Pro