Canonical Allele Identifier: CA1839089372
Gene: MTAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21816522_21816523delinsTG , CM000671.2:g.21816522_21816523delinsTG GRCh38
NC_000009.11:g.21816521_21816522delinsTG , CM000671.1:g.21816521_21816522delinsTG GRCh37
NC_000009.10:g.21806521_21806522delinsTG NCBI36
NG_032650.1:g.18887_18888delinsTG
NG_032650.2:g.18887_18888delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.121-192_121-191delinsTG ENSP00000385916.2:n.121-192_121-191delinsTG
ENST00000644715.2:c.121-192_121-191delinsTG MANE Select ENSP00000494373.1:n.121-192_121-191delinsTG
ENST00000380172.8:c.121-192_121-191delinsTG ENSP00000369519.4:n.121-192_121-191delinsTG
ENST00000404796.2:c.121-192_121-191delinsTG ENSP00000385916.2:n.121-192_121-191delinsTG
ENST00000419385.5:c.146-192_146-191delinsTG ENSP00000393507.1:n.146-192_146-191delinsTG
ENST00000427788.2:n.507-192_507-191delinsTG
ENST00000460874.6:c.172-192_172-191delinsTG ENSP00000461932.1:n.172-192_172-191delinsTG
ENST00000579422.5:n.509-192_509-191delinsTG
ENST00000580718.1:c.121-192_121-191delinsTG ENSP00000464616.1:n.121-192_121-191delinsTG
ENST00000580900.5:c.121-192_121-191delinsTG ENSP00000463424.1:n.121-192_121-191delinsTG
NM_002451.3:c.121-192_121-191delinsTG NP_002442.2:n.121-192_121-191delinsTG
NM_002451.4:c.121-192_121-191delinsTG MANE Select NP_002442.2:n.121-192_121-191delinsTG
NM_001396040.1:c.172-192_172-191delinsTG NP_001382969.1:n.172-192_172-191delinsTG
NM_001396041.1:c.121-192_121-191delinsTG NP_001382970.1:n.121-192_121-191delinsTG
NM_001396042.1:c.121-192_121-191delinsTG NP_001382971.1:n.121-192_121-191delinsTG
NM_001396043.1:c.121-192_121-191delinsTG NP_001382972.1:n.121-192_121-191delinsTG
NM_001396044.1:c.121-192_121-191delinsTG NP_001382973.1:n.121-192_121-191delinsTG
NM_001396045.1:c.121-192_121-191delinsTG NP_001382974.1:n.121-192_121-191delinsTG
NR_173242.1:n.234-192_234-191delinsTG