Canonical Allele Identifier: CA190730052

Gene: MTAP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21865788A>G , CM000671.2:g.21865788A>G	GRCh38
NC_000009.11:g.21865787A>G , CM000671.1:g.21865787A>G	GRCh37
NC_000009.10:g.21855787A>G	NCBI36
NG_032650.1:g.68153A>G
NG_032650.2:g.68153A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002451.4:c.*3774A>G MANE Select	NP_002442.2:n.*3774A>G
ENST00000644715.2:c.*3774A>G MANE Select	ENSP00000494373.1:n.*3774A>G
NM_001396040.1:c.*3774A>G	NP_001382969.1:n.*3774A>G
NM_001396041.1:c.813+6363A>G	NP_001382970.1:n.813+6363A>G
NM_001396042.1:c.690+10918A>G	NP_001382971.1:n.690+10918A>G
NM_001396043.1:c.813+6363A>G	NP_001382972.1:n.813+6363A>G
NM_001396044.1:c.813+6363A>G	NP_001382973.1:n.813+6363A>G
NM_001396045.1:c.690+10918A>G	NP_001382974.1:n.690+10918A>G
NM_002451.3:c.*3774A>G	NP_002442.2:n.*3774A>G
NR_173242.1:n.4756A>G
ENST00000380172.8:c.*3774A>G	ENSP00000369519.4:n.*3774A>G
ENST00000404796.2:c.347+47586A>G	ENSP00000385916.2:n.347+47586A>G
ENST00000404796.3:c.347+47586A>G	ENSP00000385916.2:n.347+47586A>G
ENST00000577563.1:c.147+10918A>G	ENSP00000462082.1:n.147+10918A>G
ENST00000580900.5:c.813+6363A>G	ENSP00000463424.1:n.813+6363A>G