Canonical Allele Identifier: CA1839089390
Gene: MTAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21816566_21816567delinsAT , CM000671.2:g.21816566_21816567delinsAT GRCh38
NC_000009.11:g.21816565_21816566delinsAT , CM000671.1:g.21816565_21816566delinsAT GRCh37
NC_000009.10:g.21806565_21806566delinsAT NCBI36
NG_032650.1:g.18931_18932delinsAT
NG_032650.2:g.18931_18932delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.121-148_121-147delinsAT ENSP00000385916.2:n.121-148_121-147delinsAT
ENST00000644715.2:c.121-148_121-147delinsAT MANE Select ENSP00000494373.1:n.121-148_121-147delinsAT
ENST00000380172.8:c.121-148_121-147delinsAT ENSP00000369519.4:n.121-148_121-147delinsAT
ENST00000404796.2:c.121-148_121-147delinsAT ENSP00000385916.2:n.121-148_121-147delinsAT
ENST00000419385.5:c.146-148_146-147delinsAT ENSP00000393507.1:n.146-148_146-147delinsAT
ENST00000427788.2:n.507-148_507-147delinsAT
ENST00000460874.6:c.172-148_172-147delinsAT ENSP00000461932.1:n.172-148_172-147delinsAT
ENST00000579422.5:n.509-148_509-147delinsAT
ENST00000580718.1:c.121-148_121-147delinsAT ENSP00000464616.1:n.121-148_121-147delinsAT
ENST00000580900.5:c.121-148_121-147delinsAT ENSP00000463424.1:n.121-148_121-147delinsAT
NM_002451.3:c.121-148_121-147delinsAT NP_002442.2:n.121-148_121-147delinsAT
NM_002451.4:c.121-148_121-147delinsAT MANE Select NP_002442.2:n.121-148_121-147delinsAT
NM_001396040.1:c.172-148_172-147delinsAT NP_001382969.1:n.172-148_172-147delinsAT
NM_001396041.1:c.121-148_121-147delinsAT NP_001382970.1:n.121-148_121-147delinsAT
NM_001396042.1:c.121-148_121-147delinsAT NP_001382971.1:n.121-148_121-147delinsAT
NM_001396043.1:c.121-148_121-147delinsAT NP_001382972.1:n.121-148_121-147delinsAT
NM_001396044.1:c.121-148_121-147delinsAT NP_001382973.1:n.121-148_121-147delinsAT
NM_001396045.1:c.121-148_121-147delinsAT NP_001382974.1:n.121-148_121-147delinsAT
NR_173242.1:n.234-148_234-147delinsAT