Canonical Allele Identifier: CA2806935179

Gene: ABCC11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.48224134C>T , CM000678.2:g.48224134C>T	GRCh38
NC_000016.9:g.48258045C>T , CM000678.1:g.48258045C>T	GRCh37
NC_000016.8:g.46815546C>T	NCBI36
NG_011522.1:g.16044G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356608.7:c.543+148G>A MANE Select	ENSP00000349017.2:n.543+148G>A
ENST00000353782.9:c.543+148G>A	ENSP00000311326.6:n.543+148G>A
ENST00000356608.6:c.543+148G>A	ENSP00000349017.2:n.543+148G>A
ENST00000394747.5:c.543+148G>A	ENSP00000378230.1:n.543+148G>A
ENST00000394748.5:c.543+148G>A	ENSP00000378231.1:n.543+148G>A
ENST00000567385.5:n.941+148G>A
NM_032583.3:c.543+148G>A	NP_115972.2:n.543+148G>A
NM_033151.3:c.543+148G>A	NP_149163.2:n.543+148G>A
NM_145186.2:c.543+148G>A	NP_660187.1:n.543+148G>A
XM_011523396.1:c.345+148G>A	XP_011521698.1:n.345+148G>A
XM_017023795.2:c.543+148G>A	XP_016879284.1:n.543+148G>A
XM_017023796.2:c.543+148G>A	XP_016879285.1:n.543+148G>A
XM_017023797.2:c.543+148G>A	XP_016879286.1:n.543+148G>A
XM_017023798.2:c.543+148G>A	XP_016879287.1:n.543+148G>A
XM_017023799.2:c.543+148G>A	XP_016879288.1:n.543+148G>A
XM_017023800.2:c.543+148G>A	XP_016879289.1:n.543+148G>A
XM_017023801.2:c.543+148G>A	XP_016879290.1:n.543+148G>A
XM_017023803.1:c.543+148G>A	XP_016879292.1:n.543+148G>A
XR_001752012.1:n.3221+148G>A
NM_001370496.1:c.543+148G>A	NP_001357425.1:n.543+148G>A
NM_001370497.1:c.543+148G>A MANE Select	NP_001357426.1:n.543+148G>A
NM_032583.4:c.543+148G>A	NP_115972.2:n.543+148G>A
NM_033151.4:c.543+148G>A	NP_149163.2:n.543+148G>A
NM_145186.3:c.543+148G>A	NP_660187.1:n.543+148G>A