Canonical Allele Identifier: CA478851417

Gene: ART4 C12orf60

Linked Data

• MyVariant Identifiers: chr12:g.14993794A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14840860A>G , CM000674.2:g.14840860A>G	GRCh38
NC_000012.11:g.14993794A>G , CM000674.1:g.14993794A>G	GRCh37
NC_000012.10:g.14885061A>G	NCBI36
NG_007477.2:g.7620T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000228936.6:c.438T>C (ART4) MANE Select	ENSP00000228936.4:p.Thr146=
ENST00000648334.1:n.125+11181A>G (C12orf60)
ENST00000228936.4:c.438T>C (ART4)	ENSP00000228936.4:p.Thr146=
ENST00000420600.1:c.387T>C (ART4)	ENSP00000405689.1:p.Thr129=
ENST00000430129.6:c.165+222T>C (ART4)	ENSP00000412735.2:n.165+222T>C
ENST00000527783.1:n.75+37109A>G (C12orf60)
ENST00000533472.1:n.86+37109A>G (C12orf60)
ENST00000544616.5:c.93+2110T>C (ART4)	ENSP00000442877.1:n.93+2110T>C
NM_021071.2:c.438T>C (ART4)	NP_066549.2:p.Thr146=
NM_001354646.1:c.438T>C (ART4)	NP_001341575.1:p.Thr146=
NM_021071.3:c.438T>C (ART4)	NP_066549.2:p.Thr146=
NM_021071.4:c.438T>C (ART4) MANE Select	NP_066549.2:p.Thr146=
NM_001354646.2:c.438T>C (ART4)	NP_001341575.1:p.Thr146=