Canonical Allele Identifier: CA2581072575
Gene: ART4 HGNC NCBI
C12orf60 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14840853G= , CM000674.2:g.14840853G= GRCh38
NC_000012.11:g.14993787G= , CM000674.1:g.14993787G= GRCh37
NC_000012.10:g.14885054G= NCBI36
NG_007477.2:g.7627C=

Transcript Alleles

HGVS Amino-acid change
ENST00000228936.6:c.445C= (ART4) MANE Select ENSP00000228936.4:p.Gln149=
ENST00000648334.1:n.125+11174G= (C12orf60)
ENST00000228936.4:c.445C= (ART4) ENSP00000228936.4:p.Gln149=
ENST00000420600.1:c.394C= (ART4) ENSP00000405689.1:p.Gln132=
ENST00000430129.6:c.165+229C= (ART4) ENSP00000412735.2:n.165+229C=
ENST00000527783.1:n.75+37102G= (C12orf60)
ENST00000533472.1:n.86+37102G= (C12orf60)
ENST00000544616.5:c.93+2117C= (ART4) ENSP00000442877.1:n.93+2117C=
NM_021071.2:c.445C= (ART4) NP_066549.2:p.Gln149=
NM_001354646.1:c.445C= (ART4) NP_001341575.1:p.Gln149=
NM_021071.3:c.445C= (ART4) NP_066549.2:p.Gln149=
NM_021071.4:c.445C= (ART4) MANE Select NP_066549.2:p.Gln149=
NM_001354646.2:c.445C= (ART4) NP_001341575.1:p.Gln149=