Canonical Allele Identifier: CA346664379
Gene: ABCG5 HGNC NCBI
DYNC2LI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43824084C>G , CM000664.2:g.43824084C>G GRCh38
NC_000002.11:g.44051223C>G , CM000664.1:g.44051223C>G GRCh37
NC_000002.10:g.43904727C>G NCBI36
NG_008883.1:g.19736G>C
NG_053008.1:g.55046C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000405322.8:c.1153G>C (ABCG5) MANE Select ENSP00000384513.2:p.Ala385Pro
ENST00000644754.1:n.1537G>C (ABCG5)
ENST00000260645.5:c.1153G>C (ABCG5) ENSP00000260645.1:p.Ala385Pro
ENST00000405322.5:c.640G>C (ABCG5) ENSP00000384513.1:p.Ala214Pro
ENST00000409962.1:c.*27G>C (ABCG5) ENSP00000386501.1:n.*27G>C
ENST00000486512.5:c.*422G>C (ABCG5) ENSP00000430935.1:n.*422G>C
NM_022436.2:c.1153G>C (ABCG5) NP_071881.1:p.Ala385Pro
XM_005264364.3:c.*16-3302C>G (DYNC2LI1) XP_005264421.1:n.*16-3302C>G
XM_005264365.3:c.*16-3302C>G (DYNC2LI1) XP_005264422.1:n.*16-3302C>G
XM_005264480.2:c.1153G>C (ABCG5) XP_005264537.1:p.Ala385Pro
XM_006712073.2:c.1153G>C (ABCG5) XP_006712136.1:p.Ala385Pro
XM_011533024.1:c.1153G>C (ABCG5) XP_011531326.1:p.Ala385Pro
XM_011533025.1:c.910G>C (ABCG5) XP_011531327.1:p.Ala304Pro
XM_011533026.1:c.883G>C (ABCG5) XP_011531328.1:p.Ala295Pro
XM_011533027.1:c.640G>C (ABCG5) XP_011531329.1:p.Ala214Pro
XM_011533028.1:c.316G>C (ABCG5) XP_011531330.1:p.Ala106Pro
NM_001348912.1:c.*16-3302C>G (DYNC2LI1) NP_001335841.1:n.*16-3302C>G
NM_001348913.1:c.*16-3302C>G (DYNC2LI1) NP_001335842.1:n.*16-3302C>G
XM_005264480.4:c.1153G>C (ABCG5) XP_005264537.1:p.Ala385Pro
XM_006712073.3:c.1153G>C (ABCG5) XP_006712136.1:p.Ala385Pro
XM_011533024.2:c.1153G>C (ABCG5) XP_011531326.1:p.Ala385Pro
XM_011533025.3:c.910G>C (ABCG5) XP_011531327.1:p.Ala304Pro
XM_011533026.2:c.883G>C (ABCG5) XP_011531328.1:p.Ala295Pro
XM_011533027.3:c.640G>C (ABCG5) XP_011531329.1:p.Ala214Pro
XM_011533028.2:c.316G>C (ABCG5) XP_011531330.1:p.Ala106Pro
NM_022436.3:c.1153G>C (ABCG5) MANE Select NP_071881.1:p.Ala385Pro
NM_001348912.2:c.*16-3302C>G (DYNC2LI1) NP_001335841.1:n.*16-3302C>G
NM_001348913.2:c.*16-3302C>G (DYNC2LI1) NP_001335842.1:n.*16-3302C>G