Canonical Allele Identifier: CA2689590294
Gene: MTAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21816746_21816748del , CM000671.2:g.21816746_21816748del GRCh38
NC_000009.11:g.21816745_21816747del , CM000671.1:g.21816745_21816747del GRCh37
NC_000009.10:g.21806745_21806747del NCBI36
NG_032650.1:g.19111_19113del
NG_032650.2:g.19111_19113del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.153_155del ENSP00000385916.2:p.Lys51del
ENST00000644715.2:c.153_155del MANE Select ENSP00000494373.1:p.Lys51del
ENST00000380172.8:c.153_155del ENSP00000369519.4:p.Lys51del
ENST00000404796.2:c.153_155del ENSP00000385916.2:p.Lys51del
ENST00000419385.5:c.*25_*27del ENSP00000393507.1:n.*25_*27del
ENST00000427788.2:n.539_541del
ENST00000460874.6:c.204_206del ENSP00000461932.1:p.Lys68del
ENST00000579422.5:n.541_543del
ENST00000580718.1:c.153_155del ENSP00000464616.1:p.Lys51del
ENST00000580900.5:c.153_155del ENSP00000463424.1:p.Lys51del
NM_002451.3:c.153_155del NP_002442.2:p.Lys51del
NM_002451.4:c.153_155del MANE Select NP_002442.2:p.Lys51del
NM_001396040.1:c.204_206del NP_001382969.1:p.Lys68del
NM_001396041.1:c.153_155del NP_001382970.1:p.Lys51del
NM_001396042.1:c.153_155del NP_001382971.1:p.Lys51del
NM_001396043.1:c.153_155del NP_001382972.1:p.Lys51del
NM_001396044.1:c.153_155del NP_001382973.1:p.Lys51del
NM_001396045.1:c.153_155del NP_001382974.1:p.Lys51del
NR_173242.1:n.266_268del