Canonical Allele Identifier: CA3191836598

Gene: ART4 C12orf60

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14842968A= , CM000674.2:g.14842968A=	GRCh38
NC_000012.11:g.14995902A= , CM000674.1:g.14995902A=	GRCh37
NC_000012.10:g.14887169A=	NCBI36
NG_007477.2:g.5512T=

Transcript Alleles

HGVS	Amino-acid Change
NM_021071.4:c.144+2T= (ART4) MANE Select	NP_066549.2:n.144+2T=
ENST00000228936.6:c.144+2T= (ART4) MANE Select	ENSP00000228936.4:n.144+2T=
NM_001354646.1:c.144+2T= (ART4)	NP_001341575.1:n.144+2T=
NM_001354646.2:c.144+2T= (ART4)	NP_001341575.1:n.144+2T=
NM_021071.2:c.144+2T= (ART4)	NP_066549.2:n.144+2T=
NM_021071.3:c.144+2T= (ART4)	NP_066549.2:n.144+2T=
ENST00000228936.4:c.144+2T= (ART4)	ENSP00000228936.4:n.144+2T=
ENST00000420600.1:c.93+2T= (ART4)	ENSP00000405689.1:n.93+2T=
ENST00000430129.6:c.93+2T= (ART4)	ENSP00000412735.2:n.93+2T=
ENST00000527783.1:n.75+39217A= (C12orf60)
ENST00000533472.1:n.86+39217A= (C12orf60)
ENST00000544616.5:c.93+2T= (ART4)	ENSP00000442877.1:n.93+2T=
ENST00000648334.1:n.125+13289A= (C12orf60)