Canonical Allele Identifier: CA1839089665
Gene: MTAP HGNC NCBI

Linked Data

dbSNP Id: rs1824494208

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21817081_21817084del , CM000671.2:g.21817081_21817084del GRCh38
NC_000009.11:g.21817080_21817083del , CM000671.1:g.21817080_21817083del GRCh37
NC_000009.10:g.21807080_21807083del NCBI36
NG_032650.1:g.19446_19449del
NG_032650.2:g.19446_19449del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.179+309_179+312del ENSP00000385916.2:n.179+309_179+312del
ENST00000644715.2:c.179+309_179+312del MANE Select ENSP00000494373.1:n.179+309_179+312del
ENST00000380172.8:c.179+309_179+312del ENSP00000369519.4:n.179+309_179+312del
ENST00000404796.2:c.179+309_179+312del ENSP00000385916.2:n.179+309_179+312del
ENST00000419385.5:c.*51+309_*51+312del ENSP00000393507.1:n.*51+309_*51+312del
ENST00000427788.2:n.565+309_565+312del
ENST00000460874.6:c.230+309_230+312del ENSP00000461932.1:n.230+309_230+312del
ENST00000579422.5:n.567+309_567+312del
ENST00000580718.1:c.179+309_179+312del ENSP00000464616.1:n.179+309_179+312del
ENST00000580900.5:c.179+309_179+312del ENSP00000463424.1:n.179+309_179+312del
NM_002451.3:c.179+309_179+312del NP_002442.2:n.179+309_179+312del
NM_002451.4:c.179+309_179+312del MANE Select NP_002442.2:n.179+309_179+312del
NM_001396040.1:c.230+309_230+312del NP_001382969.1:n.230+309_230+312del
NM_001396041.1:c.179+309_179+312del NP_001382970.1:n.179+309_179+312del
NM_001396042.1:c.179+309_179+312del NP_001382971.1:n.179+309_179+312del
NM_001396043.1:c.179+309_179+312del NP_001382972.1:n.179+309_179+312del
NM_001396044.1:c.179+309_179+312del NP_001382973.1:n.179+309_179+312del
NM_001396045.1:c.179+309_179+312del NP_001382974.1:n.179+309_179+312del
NR_173242.1:n.292+309_292+312del