Canonical Allele Identifier: CA1122160306
Gene: MTAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21817066_21817067insTTTTT , CM000671.2:g.21817066_21817067insTTTTT GRCh38
NC_000009.11:g.21817065_21817066insTTTTT , CM000671.1:g.21817065_21817066insTTTTT GRCh37
NC_000009.10:g.21807065_21807066insTTTTT NCBI36
NG_032650.1:g.19431_19432insTTTTT
NG_032650.2:g.19431_19432insTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.179+294_179+295insTTTTT ENSP00000385916.2:n.179+294_179+295insTTTTT
ENST00000644715.2:c.179+294_179+295insTTTTT MANE Select ENSP00000494373.1:n.179+294_179+295insTTTTT
ENST00000380172.8:c.179+294_179+295insTTTTT ENSP00000369519.4:n.179+294_179+295insTTTTT
ENST00000404796.2:c.179+294_179+295insTTTTT ENSP00000385916.2:n.179+294_179+295insTTTTT
ENST00000419385.5:c.*51+294_*51+295insTTTTT ENSP00000393507.1:n.*51+294_*51+295insTTTTT
ENST00000427788.2:n.565+294_565+295insTTTTT
ENST00000460874.6:c.230+294_230+295insTTTTT ENSP00000461932.1:n.230+294_230+295insTTTTT
ENST00000579422.5:n.567+294_567+295insTTTTT
ENST00000580718.1:c.179+294_179+295insTTTTT ENSP00000464616.1:n.179+294_179+295insTTTTT
ENST00000580900.5:c.179+294_179+295insTTTTT ENSP00000463424.1:n.179+294_179+295insTTTTT
NM_002451.3:c.179+294_179+295insTTTTT NP_002442.2:n.179+294_179+295insTTTTT
NM_002451.4:c.179+294_179+295insTTTTT MANE Select NP_002442.2:n.179+294_179+295insTTTTT
NM_001396040.1:c.230+294_230+295insTTTTT NP_001382969.1:n.230+294_230+295insTTTTT
NM_001396041.1:c.179+294_179+295insTTTTT NP_001382970.1:n.179+294_179+295insTTTTT
NM_001396042.1:c.179+294_179+295insTTTTT NP_001382971.1:n.179+294_179+295insTTTTT
NM_001396043.1:c.179+294_179+295insTTTTT NP_001382972.1:n.179+294_179+295insTTTTT
NM_001396044.1:c.179+294_179+295insTTTTT NP_001382973.1:n.179+294_179+295insTTTTT
NM_001396045.1:c.179+294_179+295insTTTTT NP_001382974.1:n.179+294_179+295insTTTTT
NR_173242.1:n.292+294_292+295insTTTTT