Canonical Allele Identifier: CA384013839

Gene: ART4 C12orf60

Linked Data

• MyVariant Identifiers: chr12:g.14993898G>T (hg19) ; chr12:g.14840964G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14840964G>T , CM000674.2:g.14840964G>T	GRCh38
NC_000012.11:g.14993898G>T , CM000674.1:g.14993898G>T	GRCh37
NC_000012.10:g.14885165G>T	NCBI36
NG_007477.2:g.7516C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000228936.6:c.334C>A (ART4) MANE Select	ENSP00000228936.4:p.Pro112Thr
ENST00000648334.1:n.125+11285G>T (C12orf60)
ENST00000228936.4:c.334C>A (ART4)	ENSP00000228936.4:p.Pro112Thr
ENST00000420600.1:c.283C>A (ART4)	ENSP00000405689.1:p.Pro95Thr
ENST00000430129.6:c.165+118C>A (ART4)	ENSP00000412735.2:n.165+118C>A
ENST00000527783.1:n.75+37213G>T (C12orf60)
ENST00000533472.1:n.86+37213G>T (C12orf60)
ENST00000544616.5:c.93+2006C>A (ART4)	ENSP00000442877.1:n.93+2006C>A
NM_021071.2:c.334C>A (ART4)	NP_066549.2:p.Pro112Thr
NM_001354646.1:c.334C>A (ART4)	NP_001341575.1:p.Pro112Thr
NM_021071.3:c.334C>A (ART4)	NP_066549.2:p.Pro112Thr
NM_021071.4:c.334C>A (ART4) MANE Select	NP_066549.2:p.Pro112Thr
NM_001354646.2:c.334C>A (ART4)	NP_001341575.1:p.Pro112Thr