Canonical Allele Identifier: CA373084988

Gene: MTAP

Linked Data

• MyVariant Identifiers: chr9:g.21816771G>C (hg19) ; chr9:g.21816772G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21816772G>C , CM000671.2:g.21816772G>C	GRCh38
NC_000009.11:g.21816771G>C , CM000671.1:g.21816771G>C	GRCh37
NC_000009.10:g.21806771G>C	NCBI36
NG_032650.1:g.19137G>C
NG_032650.2:g.19137G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.179G>C	ENSP00000385916.2:p.Arg60Thr
ENST00000644715.2:c.179G>C MANE Select	ENSP00000494373.1:p.Arg60Thr
ENST00000380172.8:c.179G>C	ENSP00000369519.4:p.Arg60Thr
ENST00000404796.2:c.179G>C	ENSP00000385916.2:p.Arg60Thr
ENST00000419385.5:c.*51G>C	ENSP00000393507.1:n.*51G>C
ENST00000427788.2:n.565G>C
ENST00000460874.6:c.230G>C	ENSP00000461932.1:p.Arg77Thr
ENST00000579422.5:n.567G>C
ENST00000580718.1:c.179G>C	ENSP00000464616.1:p.Arg60Thr
ENST00000580900.5:c.179G>C	ENSP00000463424.1:p.Arg60Thr
NM_002451.3:c.179G>C	NP_002442.2:p.Arg60Thr
NM_002451.4:c.179G>C MANE Select	NP_002442.2:p.Arg60Thr
NM_001396040.1:c.230G>C	NP_001382969.1:p.Arg77Thr
NM_001396041.1:c.179G>C	NP_001382970.1:p.Arg60Thr
NM_001396042.1:c.179G>C	NP_001382971.1:p.Arg60Thr
NM_001396043.1:c.179G>C	NP_001382972.1:p.Arg60Thr
NM_001396044.1:c.179G>C	NP_001382973.1:p.Arg60Thr
NM_001396045.1:c.179G>C	NP_001382974.1:p.Arg60Thr
NR_173242.1:n.292G>C