Canonical Allele Identifier: CA373084970
Gene: MTAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21816763T>A , CM000671.2:g.21816763T>A GRCh38
NC_000009.11:g.21816762T>A , CM000671.1:g.21816762T>A GRCh37
NC_000009.10:g.21806762T>A NCBI36
NG_032650.1:g.19128T>A
NG_032650.2:g.19128T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000404796.3:c.170T>A ENSP00000385916.2:p.Leu57His
ENST00000644715.2:c.170T>A MANE Select ENSP00000494373.1:p.Leu57His
ENST00000380172.8:c.170T>A ENSP00000369519.4:p.Leu57His
ENST00000404796.2:c.170T>A ENSP00000385916.2:p.Leu57His
ENST00000419385.5:c.*42T>A ENSP00000393507.1:n.*42T>A
ENST00000427788.2:n.556T>A
ENST00000460874.6:c.221T>A ENSP00000461932.1:p.Leu74His
ENST00000579422.5:n.558T>A
ENST00000580718.1:c.170T>A ENSP00000464616.1:p.Leu57His
ENST00000580900.5:c.170T>A ENSP00000463424.1:p.Leu57His
NM_002451.3:c.170T>A NP_002442.2:p.Leu57His
NM_002451.4:c.170T>A MANE Select NP_002442.2:p.Leu57His
NM_001396040.1:c.221T>A NP_001382969.1:p.Leu74His
NM_001396041.1:c.170T>A NP_001382970.1:p.Leu57His
NM_001396042.1:c.170T>A NP_001382971.1:p.Leu57His
NM_001396043.1:c.170T>A NP_001382972.1:p.Leu57His
NM_001396044.1:c.170T>A NP_001382973.1:p.Leu57His
NM_001396045.1:c.170T>A NP_001382974.1:p.Leu57His
NR_173242.1:n.283T>A