Canonical Allele Identifier: CA1839089646

Gene: MTAP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21817052_21817053delinsAT , CM000671.2:g.21817052_21817053delinsAT	GRCh38
NC_000009.11:g.21817051_21817052delinsAT , CM000671.1:g.21817051_21817052delinsAT	GRCh37
NC_000009.10:g.21807051_21807052delinsAT	NCBI36
NG_032650.1:g.19417_19418delinsAT
NG_032650.2:g.19417_19418delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.179+280_179+281delinsAT	ENSP00000385916.2:n.179+280_179+281delinsAT
ENST00000644715.2:c.179+280_179+281delinsAT MANE Select	ENSP00000494373.1:n.179+280_179+281delinsAT
ENST00000380172.8:c.179+280_179+281delinsAT	ENSP00000369519.4:n.179+280_179+281delinsAT
ENST00000404796.2:c.179+280_179+281delinsAT	ENSP00000385916.2:n.179+280_179+281delinsAT
ENST00000419385.5:c.*51+280_*51+281delinsAT	ENSP00000393507.1:n.*51+280_*51+281delinsAT
ENST00000427788.2:n.565+280_565+281delinsAT
ENST00000460874.6:c.230+280_230+281delinsAT	ENSP00000461932.1:n.230+280_230+281delinsAT
ENST00000579422.5:n.567+280_567+281delinsAT
ENST00000580718.1:c.179+280_179+281delinsAT	ENSP00000464616.1:n.179+280_179+281delinsAT
ENST00000580900.5:c.179+280_179+281delinsAT	ENSP00000463424.1:n.179+280_179+281delinsAT
NM_002451.3:c.179+280_179+281delinsAT	NP_002442.2:n.179+280_179+281delinsAT
NM_002451.4:c.179+280_179+281delinsAT MANE Select	NP_002442.2:n.179+280_179+281delinsAT
NM_001396040.1:c.230+280_230+281delinsAT	NP_001382969.1:n.230+280_230+281delinsAT
NM_001396041.1:c.179+280_179+281delinsAT	NP_001382970.1:n.179+280_179+281delinsAT
NM_001396042.1:c.179+280_179+281delinsAT	NP_001382971.1:n.179+280_179+281delinsAT
NM_001396043.1:c.179+280_179+281delinsAT	NP_001382972.1:n.179+280_179+281delinsAT
NM_001396044.1:c.179+280_179+281delinsAT	NP_001382973.1:n.179+280_179+281delinsAT
NM_001396045.1:c.179+280_179+281delinsAT	NP_001382974.1:n.179+280_179+281delinsAT
NR_173242.1:n.292+280_292+281delinsAT