Canonical Allele Identifier: CA1839089486

Gene: MTAP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21816749T= , CM000671.2:g.21816749T=	GRCh38
NC_000009.11:g.21816748T= , CM000671.1:g.21816748T=	GRCh37
NC_000009.10:g.21806748T=	NCBI36
NG_032650.1:g.19114T=
NG_032650.2:g.19114T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.156T=	ENSP00000385916.2:p.Asn52=
ENST00000644715.2:c.156T= MANE Select	ENSP00000494373.1:p.Asn52=
ENST00000380172.8:c.156T=	ENSP00000369519.4:p.Asn52=
ENST00000404796.2:c.156T=	ENSP00000385916.2:p.Asn52=
ENST00000419385.5:c.*28T=	ENSP00000393507.1:n.*28T=
ENST00000427788.2:n.542T=
ENST00000460874.6:c.207T=	ENSP00000461932.1:p.Asn69=
ENST00000579422.5:n.544T=
ENST00000580718.1:c.156T=	ENSP00000464616.1:p.Asn52=
ENST00000580900.5:c.156T=	ENSP00000463424.1:p.Asn52=
NM_002451.3:c.156T=	NP_002442.2:p.Asn52=
NM_002451.4:c.156T= MANE Select	NP_002442.2:p.Asn52=
NM_001396040.1:c.207T=	NP_001382969.1:p.Asn69=
NM_001396041.1:c.156T=	NP_001382970.1:p.Asn52=
NM_001396042.1:c.156T=	NP_001382971.1:p.Asn52=
NM_001396043.1:c.156T=	NP_001382972.1:p.Asn52=
NM_001396044.1:c.156T=	NP_001382973.1:p.Asn52=
NM_001396045.1:c.156T=	NP_001382974.1:p.Asn52=
NR_173242.1:n.269T=