Canonical Allele Identifier: CA1636397
Gene: ABCG5 HGNC NCBI
DYNC2LI1 HGNC NCBI

Linked Data

dbSNP Id: rs532840788
gnomAD v2: 2-44051291-C-G
gnomAD v3: 2-43824152-C-G
gnomAD v4: 2-43824152-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43824152C>G , CM000664.2:g.43824152C>G GRCh38
NC_000002.11:g.44051291C>G , CM000664.1:g.44051291C>G GRCh37
NC_000002.10:g.43904795C>G NCBI36
NG_008883.1:g.19668G>C
NG_053008.1:g.55114C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405322.8:c.1119-34G>C (ABCG5) MANE Select ENSP00000384513.2:n.1119-34G>C
ENST00000644754.1:n.1503-34G>C (ABCG5)
ENST00000260645.5:c.1119-34G>C (ABCG5) ENSP00000260645.1:n.1119-34G>C
ENST00000405322.5:c.606-34G>C (ABCG5) ENSP00000384513.1:n.606-34G>C
ENST00000409962.1:c.392-34G>C (ABCG5) ENSP00000386501.1:n.392-34G>C
ENST00000486512.5:c.*388-34G>C (ABCG5) ENSP00000430935.1:n.*388-34G>C
NM_022436.2:c.1119-34G>C (ABCG5) NP_071881.1:n.1119-34G>C
XM_005264364.3:c.*16-3234C>G (DYNC2LI1) XP_005264421.1:n.*16-3234C>G
XM_005264365.3:c.*16-3234C>G (DYNC2LI1) XP_005264422.1:n.*16-3234C>G
XM_005264480.2:c.1119-34G>C (ABCG5) XP_005264537.1:n.1119-34G>C
XM_006712073.2:c.1119-34G>C (ABCG5) XP_006712136.1:n.1119-34G>C
XM_011533024.1:c.1119-34G>C (ABCG5) XP_011531326.1:n.1119-34G>C
XM_011533025.1:c.876-34G>C (ABCG5) XP_011531327.1:n.876-34G>C
XM_011533026.1:c.849-34G>C (ABCG5) XP_011531328.1:n.849-34G>C
XM_011533027.1:c.606-34G>C (ABCG5) XP_011531329.1:n.606-34G>C
XM_011533028.1:c.282-34G>C (ABCG5) XP_011531330.1:n.282-34G>C
NM_001348912.1:c.*16-3234C>G (DYNC2LI1) NP_001335841.1:n.*16-3234C>G
NM_001348913.1:c.*16-3234C>G (DYNC2LI1) NP_001335842.1:n.*16-3234C>G
XM_005264480.4:c.1119-34G>C (ABCG5) XP_005264537.1:n.1119-34G>C
XM_006712073.3:c.1119-34G>C (ABCG5) XP_006712136.1:n.1119-34G>C
XM_011533024.2:c.1119-34G>C (ABCG5) XP_011531326.1:n.1119-34G>C
XM_011533025.3:c.876-34G>C (ABCG5) XP_011531327.1:n.876-34G>C
XM_011533026.2:c.849-34G>C (ABCG5) XP_011531328.1:n.849-34G>C
XM_011533027.3:c.606-34G>C (ABCG5) XP_011531329.1:n.606-34G>C
XM_011533028.2:c.282-34G>C (ABCG5) XP_011531330.1:n.282-34G>C
NM_022436.3:c.1119-34G>C (ABCG5) MANE Select NP_071881.1:n.1119-34G>C
NM_001348912.2:c.*16-3234C>G (DYNC2LI1) NP_001335841.1:n.*16-3234C>G
NM_001348913.2:c.*16-3234C>G (DYNC2LI1) NP_001335842.1:n.*16-3234C>G