Canonical Allele Identifier: CA1636442

Gene: ABCG5 DYNC2LI1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43824422C>T , CM000664.2:g.43824422C>T	GRCh38
NC_000002.11:g.44051561C>T , CM000664.1:g.44051561C>T	GRCh37
NC_000002.10:g.43905065C>T	NCBI36
NG_008883.1:g.19398G>A
NG_053008.1:g.55384C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022436.3:c.915G>A (ABCG5) MANE Select	NP_071881.1:p.Thr305=
ENST00000405322.8:c.915G>A (ABCG5) MANE Select	ENSP00000384513.2:p.Thr305=
NM_001348912.1:c.*16-2964C>T (DYNC2LI1)	NP_001335841.1:n.*16-2964C>T
NM_001348912.2:c.*16-2964C>T (DYNC2LI1)	NP_001335841.1:n.*16-2964C>T
NM_001348913.1:c.*16-2964C>T (DYNC2LI1)	NP_001335842.1:n.*16-2964C>T
NM_001348913.2:c.*16-2964C>T (DYNC2LI1)	NP_001335842.1:n.*16-2964C>T
NM_022436.2:c.915G>A (ABCG5)	NP_071881.1:p.Thr305=
ENST00000260645.5:c.915G>A (ABCG5)	ENSP00000260645.1:p.Thr305=
ENST00000405322.5:c.402G>A (ABCG5)	ENSP00000384513.1:p.Thr134=
ENST00000409962.1:c.392-304G>A (ABCG5)	ENSP00000386501.1:n.392-304G>A
ENST00000486512.5:c.*388-304G>A (ABCG5)	ENSP00000430935.1:n.*388-304G>A
ENST00000644754.1:n.1299G>A (ABCG5)
XM_005264364.3:c.*16-2964C>T (DYNC2LI1)	XP_005264421.1:n.*16-2964C>T
XM_005264365.3:c.*16-2964C>T (DYNC2LI1)	XP_005264422.1:n.*16-2964C>T
XM_005264480.2:c.915G>A (ABCG5)	XP_005264537.1:p.Thr305=
XM_005264480.4:c.915G>A (ABCG5)	XP_005264537.1:p.Thr305=
XM_006712073.2:c.915G>A (ABCG5)	XP_006712136.1:p.Thr305=
XM_006712073.3:c.915G>A (ABCG5)	XP_006712136.1:p.Thr305=
XM_011533024.1:c.915G>A (ABCG5)	XP_011531326.1:p.Thr305=
XM_011533024.2:c.915G>A (ABCG5)	XP_011531326.1:p.Thr305=
XM_011533025.1:c.672G>A (ABCG5)	XP_011531327.1:p.Thr224=
XM_011533025.3:c.672G>A (ABCG5)	XP_011531327.1:p.Thr224=
XM_011533026.1:c.645G>A (ABCG5)	XP_011531328.1:p.Thr215=
XM_011533026.2:c.645G>A (ABCG5)	XP_011531328.1:p.Thr215=
XM_011533027.1:c.402G>A (ABCG5)	XP_011531329.1:p.Thr134=
XM_011533027.3:c.402G>A (ABCG5)	XP_011531329.1:p.Thr134=
XM_011533028.1:c.78G>A (ABCG5)	XP_011531330.1:p.Thr26=
XM_011533028.2:c.78G>A (ABCG5)	XP_011531330.1:p.Thr26=