Canonical Allele Identifier: CA2783187874

Gene: MTAP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21816954_21816955del , CM000671.2:g.21816954_21816955del	GRCh38
NC_000009.11:g.21816953_21816954del , CM000671.1:g.21816953_21816954del	GRCh37
NC_000009.10:g.21806953_21806954del	NCBI36
NG_032650.1:g.19319_19320del
NG_032650.2:g.19319_19320del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.179+182_179+183del	ENSP00000385916.2:n.179+182_179+183del
ENST00000644715.2:c.179+182_179+183del MANE Select	ENSP00000494373.1:n.179+182_179+183del
ENST00000380172.8:c.179+182_179+183del	ENSP00000369519.4:n.179+182_179+183del
ENST00000404796.2:c.179+182_179+183del	ENSP00000385916.2:n.179+182_179+183del
ENST00000419385.5:c.*51+182_*51+183del	ENSP00000393507.1:n.*51+182_*51+183del
ENST00000427788.2:n.565+182_565+183del
ENST00000460874.6:c.230+182_230+183del	ENSP00000461932.1:n.230+182_230+183del
ENST00000579422.5:n.567+182_567+183del
ENST00000580718.1:c.179+182_179+183del	ENSP00000464616.1:n.179+182_179+183del
ENST00000580900.5:c.179+182_179+183del	ENSP00000463424.1:n.179+182_179+183del
NM_002451.3:c.179+182_179+183del	NP_002442.2:n.179+182_179+183del
NM_002451.4:c.179+182_179+183del MANE Select	NP_002442.2:n.179+182_179+183del
NM_001396040.1:c.230+182_230+183del	NP_001382969.1:n.230+182_230+183del
NM_001396041.1:c.179+182_179+183del	NP_001382970.1:n.179+182_179+183del
NM_001396042.1:c.179+182_179+183del	NP_001382971.1:n.179+182_179+183del
NM_001396043.1:c.179+182_179+183del	NP_001382972.1:n.179+182_179+183del
NM_001396044.1:c.179+182_179+183del	NP_001382973.1:n.179+182_179+183del
NM_001396045.1:c.179+182_179+183del	NP_001382974.1:n.179+182_179+183del
NR_173242.1:n.292+182_292+183del