Canonical Allele Identifier: CA862160968

Gene: MTAP

Linked Data

• dbSNP Id: rs1392070452
• gnomAD v3: 9-21816433-TC-T
• gnomAD v4: 9-21816433-TC-T
• MyVariant Identifiers: chr9:g.21816433del (hg19) ; chr9:g.21816434del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21816434del , CM000671.2:g.21816434del	GRCh38
NC_000009.11:g.21816433del , CM000671.1:g.21816433del	GRCh37
NC_000009.10:g.21806433del	NCBI36
NG_032650.1:g.18799del
NG_032650.2:g.18799del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.121-280del	ENSP00000385916.2:n.121-280del
ENST00000644715.2:c.121-280del MANE Select	ENSP00000494373.1:n.121-280del
ENST00000380172.8:c.121-280del	ENSP00000369519.4:n.121-280del
ENST00000404796.2:c.121-280del	ENSP00000385916.2:n.121-280del
ENST00000419385.5:c.146-280del	ENSP00000393507.1:n.146-280del
ENST00000427788.2:n.507-280del
ENST00000460874.6:c.172-280del	ENSP00000461932.1:n.172-280del
ENST00000579422.5:n.509-280del
ENST00000580718.1:c.121-280del	ENSP00000464616.1:n.121-280del
ENST00000580900.5:c.121-280del	ENSP00000463424.1:n.121-280del
NM_002451.3:c.121-280del	NP_002442.2:n.121-280del
NM_002451.4:c.121-280del MANE Select	NP_002442.2:n.121-280del
NM_001396040.1:c.172-280del	NP_001382969.1:n.172-280del
NM_001396041.1:c.121-280del	NP_001382970.1:n.121-280del
NM_001396042.1:c.121-280del	NP_001382971.1:n.121-280del
NM_001396043.1:c.121-280del	NP_001382972.1:n.121-280del
NM_001396044.1:c.121-280del	NP_001382973.1:n.121-280del
NM_001396045.1:c.121-280del	NP_001382974.1:n.121-280del
NR_173242.1:n.234-280del