Canonical Allele Identifier: CA951673061
Gene: UNG HGNC NCBI
ACACB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109113428G>A , CM000674.2:g.109113428G>A GRCh38
NC_000012.11:g.109551233G>A , CM000674.1:g.109551233G>A GRCh37
NC_000012.10:g.108035616G>A NCBI36
NG_046907.1:g.7245G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699563.1:c.774+9817G>A (UNG) ENSP00000514437.1:n.774+9817G>A
XM_011538259.1:c.-10+13G>A (ACACB) XP_011536561.1:n.-10+13G>A
XM_011538260.1:c.-10+13G>A (ACACB) XP_011536562.1:n.-10+13G>A
XM_011538261.1:c.-10+13G>A (ACACB) XP_011536563.1:n.-10+13G>A
XM_011538262.1:c.-10+13G>A (ACACB) XP_011536564.1:n.-10+13G>A
XM_011538263.1:c.-10+13G>A (ACACB) XP_011536565.1:n.-10+13G>A
XM_011538264.1:c.26+13G>A (ACACB) XP_011536566.1:n.26+13G>A
XM_011538265.1:c.-10+13G>A (ACACB) XP_011536567.1:n.-10+13G>A
XR_944530.1:n.738+13G>A (ACACB)
XR_944531.1:n.738+13G>A (ACACB)
XR_944532.1:n.738+13G>A (ACACB)
XR_944533.1:n.739+13G>A (ACACB)
XM_011538259.2:c.-10+13G>A (ACACB) XP_011536561.1:n.-10+13G>A
XM_011538263.3:c.-10+13G>A (ACACB) XP_011536565.1:n.-10+13G>A
XM_011538264.3:c.26+13G>A (ACACB) XP_011536566.1:n.26+13G>A
XM_011538265.2:c.-10+13G>A (ACACB) XP_011536567.1:n.-10+13G>A
XR_002957320.1:n.749+13G>A (ACACB)
XR_002957321.1:n.749+13G>A (ACACB)
XR_944530.2:n.749+13G>A (ACACB)
XR_944532.3:n.749+13G>A (ACACB)
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