Canonical Allele Identifier: CA2497029299
Community Standard Title: NM_021071.4(ART4):c.793G= (p.Asp265=)
Gene: ART4 HGNC NCBI
C12orf60 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14840505C= , CM000674.2:g.14840505C= GRCh38
NC_000012.11:g.14993439C= , CM000674.1:g.14993439C= GRCh37
NC_000012.10:g.14884706C= NCBI36
NG_007477.2:g.7975G=

Transcript Alleles

HGVS Amino-acid Change
NM_021071.4:c.793G= (ART4) MANE Select NP_066549.2:p.Asp265=
ENST00000228936.6:c.793G= (ART4) MANE Select ENSP00000228936.4:p.Asp265=
NM_001354646.1:c.793G= (ART4) NP_001341575.1:p.Asp265=
NM_001354646.2:c.793G= (ART4) NP_001341575.1:p.Asp265=
NM_021071.2:c.793G= (ART4) NP_066549.2:p.Asp265=
NM_021071.3:c.793G= (ART4) NP_066549.2:p.Asp265=
ENST00000228936.4:c.793G= (ART4) ENSP00000228936.4:p.Asp265=
ENST00000420600.1:c.742G= (ART4) ENSP00000405689.1:p.Asp248=
ENST00000430129.6:c.165+577G= (ART4) ENSP00000412735.2:n.165+577G=
ENST00000527783.1:n.75+36754C= (C12orf60)
ENST00000533472.1:n.86+36754C= (C12orf60)
ENST00000544616.5:c.93+2465G= (ART4) ENSP00000442877.1:n.93+2465G=
ENST00000648334.1:n.125+10826C= (C12orf60)