Canonical Allele Identifier: CA1839089394
Gene: MTAP HGNC NCBI

Linked Data

dbSNP Id: rs1824480758

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21816570_21816574del , CM000671.2:g.21816570_21816574del GRCh38
NC_000009.11:g.21816569_21816573del , CM000671.1:g.21816569_21816573del GRCh37
NC_000009.10:g.21806569_21806573del NCBI36
NG_032650.1:g.18935_18939del
NG_032650.2:g.18935_18939del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.121-144_121-140del ENSP00000385916.2:n.121-144_121-140del
ENST00000644715.2:c.121-144_121-140del MANE Select ENSP00000494373.1:n.121-144_121-140del
ENST00000380172.8:c.121-144_121-140del ENSP00000369519.4:n.121-144_121-140del
ENST00000404796.2:c.121-144_121-140del ENSP00000385916.2:n.121-144_121-140del
ENST00000419385.5:c.146-144_146-140del ENSP00000393507.1:n.146-144_146-140del
ENST00000427788.2:n.507-144_507-140del
ENST00000460874.6:c.172-144_172-140del ENSP00000461932.1:n.172-144_172-140del
ENST00000579422.5:n.509-144_509-140del
ENST00000580718.1:c.121-144_121-140del ENSP00000464616.1:n.121-144_121-140del
ENST00000580900.5:c.121-144_121-140del ENSP00000463424.1:n.121-144_121-140del
NM_002451.3:c.121-144_121-140del NP_002442.2:n.121-144_121-140del
NM_002451.4:c.121-144_121-140del MANE Select NP_002442.2:n.121-144_121-140del
NM_001396040.1:c.172-144_172-140del NP_001382969.1:n.172-144_172-140del
NM_001396041.1:c.121-144_121-140del NP_001382970.1:n.121-144_121-140del
NM_001396042.1:c.121-144_121-140del NP_001382971.1:n.121-144_121-140del
NM_001396043.1:c.121-144_121-140del NP_001382972.1:n.121-144_121-140del
NM_001396044.1:c.121-144_121-140del NP_001382973.1:n.121-144_121-140del
NM_001396045.1:c.121-144_121-140del NP_001382974.1:n.121-144_121-140del
NR_173242.1:n.234-144_234-140del