Canonical Allele Identifier: CA586894382

Gene: MTAP

Linked Data

• dbSNP Id: rs1338878707
• gnomAD v2: 9-21816668-GTTTT-G
• gnomAD v4: 9-21816669-GTTTT-G
• MyVariant Identifiers: chr9:g.21816669_21816672del (hg19) ; chr9:g.21816670_21816673del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21816671_21816674del , CM000671.2:g.21816671_21816674del	GRCh38
NC_000009.11:g.21816670_21816673del , CM000671.1:g.21816670_21816673del	GRCh37
NC_000009.10:g.21806670_21806673del	NCBI36
NG_032650.1:g.19036_19039del
NG_032650.2:g.19036_19039del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.121-43_121-40del	ENSP00000385916.2:n.121-43_121-40del
ENST00000644715.2:c.121-43_121-40del MANE Select	ENSP00000494373.1:n.121-43_121-40del
ENST00000380172.8:c.121-43_121-40del	ENSP00000369519.4:n.121-43_121-40del
ENST00000404796.2:c.121-43_121-40del	ENSP00000385916.2:n.121-43_121-40del
ENST00000419385.5:c.146-43_146-40del	ENSP00000393507.1:n.146-43_146-40del
ENST00000427788.2:n.507-43_507-40del
ENST00000460874.6:c.172-43_172-40del	ENSP00000461932.1:n.172-43_172-40del
ENST00000579422.5:n.509-43_509-40del
ENST00000580718.1:c.121-43_121-40del	ENSP00000464616.1:n.121-43_121-40del
ENST00000580900.5:c.121-43_121-40del	ENSP00000463424.1:n.121-43_121-40del
NM_002451.3:c.121-43_121-40del	NP_002442.2:n.121-43_121-40del
NM_002451.4:c.121-43_121-40del MANE Select	NP_002442.2:n.121-43_121-40del
NM_001396040.1:c.172-43_172-40del	NP_001382969.1:n.172-43_172-40del
NM_001396041.1:c.121-43_121-40del	NP_001382970.1:n.121-43_121-40del
NM_001396042.1:c.121-43_121-40del	NP_001382971.1:n.121-43_121-40del
NM_001396043.1:c.121-43_121-40del	NP_001382972.1:n.121-43_121-40del
NM_001396044.1:c.121-43_121-40del	NP_001382973.1:n.121-43_121-40del
NM_001396045.1:c.121-43_121-40del	NP_001382974.1:n.121-43_121-40del
NR_173242.1:n.234-43_234-40del