Canonical Allele Identifier: CA373084885

Gene: MTAP

Linked Data

• gnomAD v4: 9-21816724-C-T
• MyVariant Identifiers: chr9:g.21816723C>T (hg19) ; chr9:g.21816724C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21816724C>T , CM000671.2:g.21816724C>T	GRCh38
NC_000009.11:g.21816723C>T , CM000671.1:g.21816723C>T	GRCh37
NC_000009.10:g.21806723C>T	NCBI36
NG_032650.1:g.19089C>T
NG_032650.2:g.19089C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.131C>T	ENSP00000385916.2:p.Ala44Val
ENST00000644715.2:c.131C>T MANE Select	ENSP00000494373.1:p.Ala44Val
ENST00000380172.8:c.131C>T	ENSP00000369519.4:p.Ala44Val
ENST00000404796.2:c.131C>T	ENSP00000385916.2:p.Ala44Val
ENST00000419385.5:c.*3C>T	ENSP00000393507.1:n.*3C>T
ENST00000427788.2:n.517C>T
ENST00000460874.6:c.182C>T	ENSP00000461932.1:p.Ala61Val
ENST00000579422.5:n.519C>T
ENST00000580718.1:c.131C>T	ENSP00000464616.1:p.Ala44Val
ENST00000580900.5:c.131C>T	ENSP00000463424.1:p.Ala44Val
NM_002451.3:c.131C>T	NP_002442.2:p.Ala44Val
NM_002451.4:c.131C>T MANE Select	NP_002442.2:p.Ala44Val
NM_001396040.1:c.182C>T	NP_001382969.1:p.Ala61Val
NM_001396041.1:c.131C>T	NP_001382970.1:p.Ala44Val
NM_001396042.1:c.131C>T	NP_001382971.1:p.Ala44Val
NM_001396043.1:c.131C>T	NP_001382972.1:p.Ala44Val
NM_001396044.1:c.131C>T	NP_001382973.1:p.Ala44Val
NM_001396045.1:c.131C>T	NP_001382974.1:p.Ala44Val
NR_173242.1:n.244C>T