Canonical Allele Identifier: CA346662728
Community Standard Title: NM_022436.3(ABCG5):c.1657C>T (p.Gln553Ter)
Gene: ABCG5 HGNC NCBI
DYNC2LI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43814582G>A , CM000664.2:g.43814582G>A GRCh38
NC_000002.11:g.44041721G>A , CM000664.1:g.44041721G>A GRCh37
NC_000002.10:g.43895225G>A NCBI36
NG_008883.1:g.29238C>T
NG_053008.1:g.45544G>A

Transcript Alleles

HGVS Amino-acid Change
NM_022436.3:c.1657C>T (ABCG5) MANE Select NP_071881.1:p.Gln553Ter
ENST00000405322.8:c.1657C>T (ABCG5) MANE Select ENSP00000384513.2:p.Gln553Ter
NM_001348912.1:c.*15+4058G>A (DYNC2LI1) NP_001335841.1:n.*15+4058G>A
NM_001348912.2:c.*15+4058G>A (DYNC2LI1) NP_001335841.1:n.*15+4058G>A
NM_001348913.1:c.*15+4058G>A (DYNC2LI1) NP_001335842.1:n.*15+4058G>A
NM_001348913.2:c.*15+4058G>A (DYNC2LI1) NP_001335842.1:n.*15+4058G>A
NM_022436.2:c.1657C>T (ABCG5) NP_071881.1:p.Gln553Ter
ENST00000260645.5:c.1657C>T (ABCG5) ENSP00000260645.1:p.Gln553Ter
ENST00000405322.5:c.1144C>T (ABCG5) ENSP00000384513.1:p.Gln382Ter
ENST00000409962.1:c.*531C>T (ABCG5) ENSP00000386501.1:n.*531C>T
ENST00000486512.5:c.*926C>T (ABCG5) ENSP00000430935.1:n.*926C>T
ENST00000644754.1:n.2041C>T (ABCG5)
XM_005264364.3:c.*15+4058G>A (DYNC2LI1) XP_005264421.1:n.*15+4058G>A
XM_005264365.3:c.*15+4058G>A (DYNC2LI1) XP_005264422.1:n.*15+4058G>A
XM_005264480.2:c.1650-1273C>T (ABCG5) XP_005264537.1:n.1650-1273C>T
XM_005264480.4:c.1650-1273C>T (ABCG5) XP_005264537.1:n.1650-1273C>T
XM_006712073.2:c.1657C>T (ABCG5) XP_006712136.1:p.Gln553Ter
XM_006712073.3:c.1657C>T (ABCG5) XP_006712136.1:p.Gln553Ter
XM_011533024.1:c.1522C>T (ABCG5) XP_011531326.1:p.Gln508Ter
XM_011533024.2:c.1522C>T (ABCG5) XP_011531326.1:p.Gln508Ter
XM_011533025.1:c.1414C>T (ABCG5) XP_011531327.1:p.Gln472Ter
XM_011533025.3:c.1414C>T (ABCG5) XP_011531327.1:p.Gln472Ter
XM_011533026.1:c.1387C>T (ABCG5) XP_011531328.1:p.Gln463Ter
XM_011533026.2:c.1387C>T (ABCG5) XP_011531328.1:p.Gln463Ter
XM_011533027.1:c.1144C>T (ABCG5) XP_011531329.1:p.Gln382Ter
XM_011533027.3:c.1144C>T (ABCG5) XP_011531329.1:p.Gln382Ter
XM_011533028.1:c.820C>T (ABCG5) XP_011531330.1:p.Gln274Ter
XM_011533028.2:c.820C>T (ABCG5) XP_011531330.1:p.Gln274Ter