Canonical Allele Identifier: CA346664362
Gene: ABCG5 HGNC NCBI
DYNC2LI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.43824075T>G , CM000664.2:g.43824075T>G GRCh38
NC_000002.11:g.44051214T>G , CM000664.1:g.44051214T>G GRCh37
NC_000002.10:g.43904718T>G NCBI36
NG_008883.1:g.19745A>C
NG_053008.1:g.55037T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000405322.8:c.1162A>C (ABCG5) MANE Select ENSP00000384513.2:p.Thr388Pro
ENST00000644754.1:n.1546A>C (ABCG5)
ENST00000260645.5:c.1162A>C (ABCG5) ENSP00000260645.1:p.Thr388Pro
ENST00000405322.5:c.649A>C (ABCG5) ENSP00000384513.1:p.Thr217Pro
ENST00000409962.1:c.*36A>C (ABCG5) ENSP00000386501.1:n.*36A>C
ENST00000486512.5:c.*431A>C (ABCG5) ENSP00000430935.1:n.*431A>C
NM_022436.2:c.1162A>C (ABCG5) NP_071881.1:p.Thr388Pro
XM_005264364.3:c.*16-3311T>G (DYNC2LI1) XP_005264421.1:n.*16-3311T>G
XM_005264365.3:c.*16-3311T>G (DYNC2LI1) XP_005264422.1:n.*16-3311T>G
XM_005264480.2:c.1162A>C (ABCG5) XP_005264537.1:p.Thr388Pro
XM_006712073.2:c.1162A>C (ABCG5) XP_006712136.1:p.Thr388Pro
XM_011533024.1:c.1162A>C (ABCG5) XP_011531326.1:p.Thr388Pro
XM_011533025.1:c.919A>C (ABCG5) XP_011531327.1:p.Thr307Pro
XM_011533026.1:c.892A>C (ABCG5) XP_011531328.1:p.Thr298Pro
XM_011533027.1:c.649A>C (ABCG5) XP_011531329.1:p.Thr217Pro
XM_011533028.1:c.325A>C (ABCG5) XP_011531330.1:p.Thr109Pro
NM_001348912.1:c.*16-3311T>G (DYNC2LI1) NP_001335841.1:n.*16-3311T>G
NM_001348913.1:c.*16-3311T>G (DYNC2LI1) NP_001335842.1:n.*16-3311T>G
XM_005264480.4:c.1162A>C (ABCG5) XP_005264537.1:p.Thr388Pro
XM_006712073.3:c.1162A>C (ABCG5) XP_006712136.1:p.Thr388Pro
XM_011533024.2:c.1162A>C (ABCG5) XP_011531326.1:p.Thr388Pro
XM_011533025.3:c.919A>C (ABCG5) XP_011531327.1:p.Thr307Pro
XM_011533026.2:c.892A>C (ABCG5) XP_011531328.1:p.Thr298Pro
XM_011533027.3:c.649A>C (ABCG5) XP_011531329.1:p.Thr217Pro
XM_011533028.2:c.325A>C (ABCG5) XP_011531330.1:p.Thr109Pro
NM_022436.3:c.1162A>C (ABCG5) MANE Select NP_071881.1:p.Thr388Pro
NM_001348912.2:c.*16-3311T>G (DYNC2LI1) NP_001335841.1:n.*16-3311T>G
NM_001348913.2:c.*16-3311T>G (DYNC2LI1) NP_001335842.1:n.*16-3311T>G