Canonical Allele Identifier: CA1122160303

Gene: MTAP

Linked Data

• gnomAD v3: 9-21817059-TCCCCC-T
• gnomAD v4: 9-21817059-TCCCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21817060_21817064del , CM000671.2:g.21817060_21817064del	GRCh38
NC_000009.11:g.21817059_21817063del , CM000671.1:g.21817059_21817063del	GRCh37
NC_000009.10:g.21807059_21807063del	NCBI36
NG_032650.1:g.19425_19429del
NG_032650.2:g.19425_19429del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.179+288_179+292del	ENSP00000385916.2:n.179+288_179+292del
ENST00000644715.2:c.179+288_179+292del MANE Select	ENSP00000494373.1:n.179+288_179+292del
ENST00000380172.8:c.179+288_179+292del	ENSP00000369519.4:n.179+288_179+292del
ENST00000404796.2:c.179+288_179+292del	ENSP00000385916.2:n.179+288_179+292del
ENST00000419385.5:c.*51+288_*51+292del	ENSP00000393507.1:n.*51+288_*51+292del
ENST00000427788.2:n.565+288_565+292del
ENST00000460874.6:c.230+288_230+292del	ENSP00000461932.1:n.230+288_230+292del
ENST00000579422.5:n.567+288_567+292del
ENST00000580718.1:c.179+288_179+292del	ENSP00000464616.1:n.179+288_179+292del
ENST00000580900.5:c.179+288_179+292del	ENSP00000463424.1:n.179+288_179+292del
NM_002451.3:c.179+288_179+292del	NP_002442.2:n.179+288_179+292del
NM_002451.4:c.179+288_179+292del MANE Select	NP_002442.2:n.179+288_179+292del
NM_001396040.1:c.230+288_230+292del	NP_001382969.1:n.230+288_230+292del
NM_001396041.1:c.179+288_179+292del	NP_001382970.1:n.179+288_179+292del
NM_001396042.1:c.179+288_179+292del	NP_001382971.1:n.179+288_179+292del
NM_001396043.1:c.179+288_179+292del	NP_001382972.1:n.179+288_179+292del
NM_001396044.1:c.179+288_179+292del	NP_001382973.1:n.179+288_179+292del
NM_001396045.1:c.179+288_179+292del	NP_001382974.1:n.179+288_179+292del
NR_173242.1:n.292+288_292+292del