Canonical Allele Identifier: CA346662431

Gene: ABCG5 DYNC2LI1

Linked Data

• dbSNP Id: rs144973796
• MyVariant Identifiers: chr2:g.44041634C>G (hg19) ; chr2:g.43814495C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43814495C>G , CM000664.2:g.43814495C>G	GRCh38
NC_000002.11:g.44041634C>G , CM000664.1:g.44041634C>G	GRCh37
NC_000002.10:g.43895138C>G	NCBI36
NG_008883.1:g.29325G>C
NG_053008.1:g.45457C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405322.8:c.1744G>C (ABCG5) MANE Select	ENSP00000384513.2:p.Gly582Arg
ENST00000644754.1:n.2128G>C (ABCG5)
ENST00000260645.5:c.1744G>C (ABCG5)	ENSP00000260645.1:p.Gly582Arg
ENST00000405322.5:c.1231G>C (ABCG5)	ENSP00000384513.1:p.Gly411Arg
ENST00000409962.1:c.*618G>C (ABCG5)	ENSP00000386501.1:n.*618G>C
ENST00000486512.5:c.*1013G>C (ABCG5)	ENSP00000430935.1:n.*1013G>C
NM_022436.2:c.1744G>C (ABCG5)	NP_071881.1:p.Gly582Arg
XM_005264364.3:c.*15+3971C>G (DYNC2LI1)	XP_005264421.1:n.*15+3971C>G
XM_005264365.3:c.*15+3971C>G (DYNC2LI1)	XP_005264422.1:n.*15+3971C>G
XM_005264480.2:c.1650-1186G>C (ABCG5)	XP_005264537.1:n.1650-1186G>C
XM_006712073.2:c.1744G>C (ABCG5)	XP_006712136.1:p.Gly582Arg
XM_011533024.1:c.1609G>C (ABCG5)	XP_011531326.1:p.Gly537Arg
XM_011533025.1:c.1501G>C (ABCG5)	XP_011531327.1:p.Gly501Arg
XM_011533026.1:c.1474G>C (ABCG5)	XP_011531328.1:p.Gly492Arg
XM_011533027.1:c.1231G>C (ABCG5)	XP_011531329.1:p.Gly411Arg
XM_011533028.1:c.907G>C (ABCG5)	XP_011531330.1:p.Gly303Arg
NM_001348912.1:c.*15+3971C>G (DYNC2LI1)	NP_001335841.1:n.*15+3971C>G
NM_001348913.1:c.*15+3971C>G (DYNC2LI1)	NP_001335842.1:n.*15+3971C>G
XM_005264480.4:c.1650-1186G>C (ABCG5)	XP_005264537.1:n.1650-1186G>C
XM_006712073.3:c.1744G>C (ABCG5)	XP_006712136.1:p.Gly582Arg
XM_011533024.2:c.1609G>C (ABCG5)	XP_011531326.1:p.Gly537Arg
XM_011533025.3:c.1501G>C (ABCG5)	XP_011531327.1:p.Gly501Arg
XM_011533026.2:c.1474G>C (ABCG5)	XP_011531328.1:p.Gly492Arg
XM_011533027.3:c.1231G>C (ABCG5)	XP_011531329.1:p.Gly411Arg
XM_011533028.2:c.907G>C (ABCG5)	XP_011531330.1:p.Gly303Arg
NM_022436.3:c.1744G>C (ABCG5) MANE Select	NP_071881.1:p.Gly582Arg
NM_001348912.2:c.*15+3971C>G (DYNC2LI1)	NP_001335841.1:n.*15+3971C>G
NM_001348913.2:c.*15+3971C>G (DYNC2LI1)	NP_001335842.1:n.*15+3971C>G