Canonical Allele Identifier: CA3191836597
Community Standard Title: NM_021071.4(ART4):c.145-2A=
Gene: ART4 HGNC NCBI
C12orf60 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14841155T= , CM000674.2:g.14841155T= GRCh38
NC_000012.11:g.14994089T= , CM000674.1:g.14994089T= GRCh37
NC_000012.10:g.14885356T= NCBI36
NG_007477.2:g.7325A=

Transcript Alleles

HGVS Amino-acid Change
NM_021071.4:c.145-2A= (ART4) MANE Select NP_066549.2:n.145-2A=
ENST00000228936.6:c.145-2A= (ART4) MANE Select ENSP00000228936.4:n.145-2A=
NM_001354646.1:c.145-2A= (ART4) NP_001341575.1:n.145-2A=
NM_001354646.2:c.145-2A= (ART4) NP_001341575.1:n.145-2A=
NM_021071.2:c.145-2A= (ART4) NP_066549.2:n.145-2A=
NM_021071.3:c.145-2A= (ART4) NP_066549.2:n.145-2A=
ENST00000228936.4:c.145-2A= (ART4) ENSP00000228936.4:n.145-2A=
ENST00000420600.1:c.94-2A= (ART4) ENSP00000405689.1:n.94-2A=
ENST00000430129.6:c.94-2A= (ART4) ENSP00000412735.2:n.94-2A=
ENST00000527783.1:n.75+37404T= (C12orf60)
ENST00000533472.1:n.86+37404T= (C12orf60)
ENST00000544616.5:c.93+1815A= (ART4) ENSP00000442877.1:n.93+1815A=
ENST00000648334.1:n.125+11476T= (C12orf60)