Canonical Allele Identifier: CA210960
Gene: ART4 HGNC NCBI

Linked Data

ClinVar Variation Id: 17731
ClinVar RCV Id: RCV000019305
dbSNP Id: rs587777831

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14841155T>C , CM000674.2:g.14841155T>C GRCh38
NC_000012.11:g.14994089T>C , CM000674.1:g.14994089T>C GRCh37
NC_000012.10:g.14885356T>C NCBI36
NG_007477.2:g.7325A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000228936.6:c.145-2A>G MANE Select ENSP00000228936.4:p.=
ENST00000648334.1:n.125+11476T>C
ENST00000228936.4:c.145-2A>G ENSP00000228936.4:p.=
ENST00000420600.1:n.94-2A>G ENSP00000405689.1:p.=
ENST00000430129.6:n.94-2A>G ENSP00000412735.2:p.=
ENST00000527783.1:n.75+37404T>C
ENST00000533472.1:n.86+37404T>C
ENST00000544616.5:n.93+1815A>G ENSP00000442877.1:p.=
NM_021071.2:c.145-2A>G NP_066549.2:p.=
NM_001354646.1:c.145-2A>G NP_001341575.1:p.=
NM_021071.3:c.145-2A>G NP_066549.2:p.=
NM_021071.4:c.145-2A>G MANE Select NP_066549.2:p.=
NM_001354646.2:c.145-2A>G NP_001341575.1:p.=