Canonical Allele Identifier: CA2493933429

Gene: ABCG5 DYNC2LI1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43823977T= , CM000664.2:g.43823977T=	GRCh38
NC_000002.11:g.44051116T= , CM000664.1:g.44051116T=	GRCh37
NC_000002.10:g.43904620T=	NCBI36
NG_008883.1:g.19843A=
NG_053008.1:g.54939T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405322.8:c.1260A= (ABCG5) MANE Select	ENSP00000384513.2:p.Val420=
ENST00000644754.1:n.1644A= (ABCG5)
ENST00000260645.5:c.1260A= (ABCG5)	ENSP00000260645.1:p.Val420=
ENST00000405322.5:c.747A= (ABCG5)	ENSP00000384513.1:p.Val249=
ENST00000409962.1:c.*134A= (ABCG5)	ENSP00000386501.1:n.*134A=
ENST00000486512.5:c.*529A= (ABCG5)	ENSP00000430935.1:n.*529A=
NM_022436.2:c.1260A= (ABCG5)	NP_071881.1:p.Val420=
XM_005264364.3:c.*16-3409T= (DYNC2LI1)	XP_005264421.1:n.*16-3409T=
XM_005264365.3:c.*16-3409T= (DYNC2LI1)	XP_005264422.1:n.*16-3409T=
XM_005264480.2:c.1260A= (ABCG5)	XP_005264537.1:p.Val420=
XM_006712073.2:c.1260A= (ABCG5)	XP_006712136.1:p.Val420=
XM_011533024.1:c.1189+71A= (ABCG5)	XP_011531326.1:n.1189+71A=
XM_011533025.1:c.1017A= (ABCG5)	XP_011531327.1:p.Val339=
XM_011533026.1:c.990A= (ABCG5)	XP_011531328.1:p.Val330=
XM_011533027.1:c.747A= (ABCG5)	XP_011531329.1:p.Val249=
XM_011533028.1:c.423A= (ABCG5)	XP_011531330.1:p.Val141=
NM_001348912.1:c.*16-3409T= (DYNC2LI1)	NP_001335841.1:n.*16-3409T=
NM_001348913.1:c.*16-3409T= (DYNC2LI1)	NP_001335842.1:n.*16-3409T=
XM_005264480.4:c.1260A= (ABCG5)	XP_005264537.1:p.Val420=
XM_006712073.3:c.1260A= (ABCG5)	XP_006712136.1:p.Val420=
XM_011533024.2:c.1189+71A= (ABCG5)	XP_011531326.1:n.1189+71A=
XM_011533025.3:c.1017A= (ABCG5)	XP_011531327.1:p.Val339=
XM_011533026.2:c.990A= (ABCG5)	XP_011531328.1:p.Val330=
XM_011533027.3:c.747A= (ABCG5)	XP_011531329.1:p.Val249=
XM_011533028.2:c.423A= (ABCG5)	XP_011531330.1:p.Val141=
NM_022436.3:c.1260A= (ABCG5) MANE Select	NP_071881.1:p.Val420=
NM_001348912.2:c.*16-3409T= (DYNC2LI1)	NP_001335841.1:n.*16-3409T=
NM_001348913.2:c.*16-3409T= (DYNC2LI1)	NP_001335842.1:n.*16-3409T=