Canonical Allele Identifier: CA384013627

Gene: ART4 C12orf60

Linked Data

• MyVariant Identifiers: chr12:g.14993799T>A (hg19) ; chr12:g.14840865T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14840865T>A , CM000674.2:g.14840865T>A	GRCh38
NC_000012.11:g.14993799T>A , CM000674.1:g.14993799T>A	GRCh37
NC_000012.10:g.14885066T>A	NCBI36
NG_007477.2:g.7615A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000228936.6:c.433A>T (ART4) MANE Select	ENSP00000228936.4:p.Arg145Trp
ENST00000648334.1:n.125+11186T>A (C12orf60)
ENST00000228936.4:c.433A>T (ART4)	ENSP00000228936.4:p.Arg145Trp
ENST00000420600.1:c.382A>T (ART4)	ENSP00000405689.1:p.Arg128Trp
ENST00000430129.6:c.165+217A>T (ART4)	ENSP00000412735.2:n.165+217A>T
ENST00000527783.1:n.75+37114T>A (C12orf60)
ENST00000533472.1:n.86+37114T>A (C12orf60)
ENST00000544616.5:c.93+2105A>T (ART4)	ENSP00000442877.1:n.93+2105A>T
NM_021071.2:c.433A>T (ART4)	NP_066549.2:p.Arg145Trp
NM_001354646.1:c.433A>T (ART4)	NP_001341575.1:p.Arg145Trp
NM_021071.3:c.433A>T (ART4)	NP_066549.2:p.Arg145Trp
NM_021071.4:c.433A>T (ART4) MANE Select	NP_066549.2:p.Arg145Trp
NM_001354646.2:c.433A>T (ART4)	NP_001341575.1:p.Arg145Trp