Canonical Allele Identifier: CA15600684
Gene: MTAP HGNC NCBI

Linked Data

dbSNP Id: rs10757257
gnomAD v2: 9-21806564-G-A
gnomAD v3: 9-21806565-G-A
gnomAD v4: 9-21806565-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21806565G>A , CM000671.2:g.21806565G>A GRCh38
NC_000009.11:g.21806564G>A , CM000671.1:g.21806564G>A GRCh37
NC_000009.10:g.21796564G>A NCBI36
NG_032650.1:g.8930G>A
NG_032650.2:g.8930G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000404796.3:c.33+3784G>A ENSP00000385916.2:n.33+3784G>A
ENST00000644715.2:c.33+3784G>A MANE Select ENSP00000494373.1:n.33+3784G>A
ENST00000380172.8:c.33+3784G>A ENSP00000369519.4:n.33+3784G>A
ENST00000404796.2:c.33+3784G>A ENSP00000385916.2:n.33+3784G>A
ENST00000419385.5:c.33+3784G>A ENSP00000393507.1:n.33+3784G>A
ENST00000427788.2:n.105-2242G>A
ENST00000460874.6:c.84+3615G>A ENSP00000461932.1:n.84+3615G>A
ENST00000579422.5:n.421+3184G>A
ENST00000580675.1:n.135+3784G>A
ENST00000580718.1:c.33+3784G>A ENSP00000464616.1:n.33+3784G>A
ENST00000580900.5:c.33+3784G>A ENSP00000463424.1:n.33+3784G>A
NM_002451.3:c.33+3784G>A NP_002442.2:n.33+3784G>A
NM_002451.4:c.33+3784G>A MANE Select NP_002442.2:n.33+3784G>A
NM_001396040.1:c.84+3615G>A NP_001382969.1:n.84+3615G>A
NM_001396041.1:c.33+3784G>A NP_001382970.1:n.33+3784G>A
NM_001396042.1:c.33+3784G>A NP_001382971.1:n.33+3784G>A
NM_001396043.1:c.33+3784G>A NP_001382972.1:n.33+3784G>A
NM_001396044.1:c.33+3784G>A NP_001382973.1:n.33+3784G>A
NM_001396045.1:c.33+3784G>A NP_001382974.1:n.33+3784G>A
NR_173242.1:n.146+3784G>A