Canonical Allele Identifier: CA586894394

Gene: MTAP

Linked Data

• dbSNP Id: rs1242832917
• gnomAD v2: 9-21816741-TA-T
• gnomAD v4: 9-21816742-TA-T
• MyVariant Identifiers: chr9:g.21816742del (hg19) ; chr9:g.21816743del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21816748del , CM000671.2:g.21816748del	GRCh38
NC_000009.11:g.21816747del , CM000671.1:g.21816747del	GRCh37
NC_000009.10:g.21806747del	NCBI36
NG_032650.1:g.19113del
NG_032650.2:g.19113del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.155del	ENSP00000385916.2:p.Asn52MetfsTer30
ENST00000644715.2:c.155del MANE Select	ENSP00000494373.1:p.Asn52MetfsTer30
ENST00000380172.8:c.155del	ENSP00000369519.4:p.Asn52MetfsTer30
ENST00000404796.2:c.155del	ENSP00000385916.2:p.Asn52MetfsTer30
ENST00000419385.5:c.*27del	ENSP00000393507.1:n.*27del
ENST00000427788.2:n.541del
ENST00000460874.6:c.206del	ENSP00000461932.1:p.Asn69MetfsTer30
ENST00000579422.5:n.543del
ENST00000580718.1:c.155del	ENSP00000464616.1:p.Asn52MetfsTer30
ENST00000580900.5:c.155del	ENSP00000463424.1:p.Asn52MetfsTer30
NM_002451.3:c.155del	NP_002442.2:p.Asn52MetfsTer30
NM_002451.4:c.155del MANE Select	NP_002442.2:p.Asn52MetfsTer30
NM_001396040.1:c.206del	NP_001382969.1:p.Asn69MetfsTer30
NM_001396041.1:c.155del	NP_001382970.1:p.Asn52MetfsTer30
NM_001396042.1:c.155del	NP_001382971.1:p.Asn52MetfsTer30
NM_001396043.1:c.155del	NP_001382972.1:p.Asn52MetfsTer30
NM_001396044.1:c.155del	NP_001382973.1:p.Asn52MetfsTer30
NM_001396045.1:c.155del	NP_001382974.1:p.Asn52MetfsTer30
NR_173242.1:n.268del