Canonical Allele Identifier: CA425871661

Gene: ABCG5 DYNC2LI1

Linked Data

• MyVariant Identifiers: chr2:g.44051221T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43824082T>G , CM000664.2:g.43824082T>G	GRCh38
NC_000002.11:g.44051221T>G , CM000664.1:g.44051221T>G	GRCh37
NC_000002.10:g.43904725T>G	NCBI36
NG_008883.1:g.19738A>C
NG_053008.1:g.55044T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405322.8:c.1155A>C (ABCG5) MANE Select	ENSP00000384513.2:p.Ala385=
ENST00000644754.1:n.1539A>C (ABCG5)
ENST00000260645.5:c.1155A>C (ABCG5)	ENSP00000260645.1:p.Ala385=
ENST00000405322.5:c.642A>C (ABCG5)	ENSP00000384513.1:p.Ala214=
ENST00000409962.1:c.*29A>C (ABCG5)	ENSP00000386501.1:n.*29A>C
ENST00000486512.5:c.*424A>C (ABCG5)	ENSP00000430935.1:n.*424A>C
NM_022436.2:c.1155A>C (ABCG5)	NP_071881.1:p.Ala385=
XM_005264364.3:c.*16-3304T>G (DYNC2LI1)	XP_005264421.1:n.*16-3304T>G
XM_005264365.3:c.*16-3304T>G (DYNC2LI1)	XP_005264422.1:n.*16-3304T>G
XM_005264480.2:c.1155A>C (ABCG5)	XP_005264537.1:p.Ala385=
XM_006712073.2:c.1155A>C (ABCG5)	XP_006712136.1:p.Ala385=
XM_011533024.1:c.1155A>C (ABCG5)	XP_011531326.1:p.Ala385=
XM_011533025.1:c.912A>C (ABCG5)	XP_011531327.1:p.Ala304=
XM_011533026.1:c.885A>C (ABCG5)	XP_011531328.1:p.Ala295=
XM_011533027.1:c.642A>C (ABCG5)	XP_011531329.1:p.Ala214=
XM_011533028.1:c.318A>C (ABCG5)	XP_011531330.1:p.Ala106=
NM_001348912.1:c.*16-3304T>G (DYNC2LI1)	NP_001335841.1:n.*16-3304T>G
NM_001348913.1:c.*16-3304T>G (DYNC2LI1)	NP_001335842.1:n.*16-3304T>G
XM_005264480.4:c.1155A>C (ABCG5)	XP_005264537.1:p.Ala385=
XM_006712073.3:c.1155A>C (ABCG5)	XP_006712136.1:p.Ala385=
XM_011533024.2:c.1155A>C (ABCG5)	XP_011531326.1:p.Ala385=
XM_011533025.3:c.912A>C (ABCG5)	XP_011531327.1:p.Ala304=
XM_011533026.2:c.885A>C (ABCG5)	XP_011531328.1:p.Ala295=
XM_011533027.3:c.642A>C (ABCG5)	XP_011531329.1:p.Ala214=
XM_011533028.2:c.318A>C (ABCG5)	XP_011531330.1:p.Ala106=
NM_022436.3:c.1155A>C (ABCG5) MANE Select	NP_071881.1:p.Ala385=
NM_001348912.2:c.*16-3304T>G (DYNC2LI1)	NP_001335841.1:n.*16-3304T>G
NM_001348913.2:c.*16-3304T>G (DYNC2LI1)	NP_001335842.1:n.*16-3304T>G