Canonical Allele Identifier: CA1839116398
Gene: MTAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.21864830G= , CM000671.2:g.21864830G= GRCh38
NC_000009.11:g.21864829G= , CM000671.1:g.21864829G= GRCh37
NC_000009.10:g.21854829G= NCBI36
NG_032650.1:g.67195G=
NG_032650.2:g.67195G=

Transcript Alleles

HGVS Amino-acid change
ENST00000404796.3:c.347+46628G= ENSP00000385916.2:n.347+46628G=
ENST00000644715.2:c.*2816G= MANE Select ENSP00000494373.1:n.*2816G=
ENST00000380172.8:c.*2816G= ENSP00000369519.4:n.*2816G=
ENST00000404796.2:c.347+46628G= ENSP00000385916.2:n.347+46628G=
ENST00000577563.1:c.147+9960G= ENSP00000462082.1:n.147+9960G=
ENST00000580900.5:c.813+5405G= ENSP00000463424.1:n.813+5405G=
NM_002451.3:c.*2816G= NP_002442.2:n.*2816G=
NM_002451.4:c.*2816G= MANE Select NP_002442.2:n.*2816G=
NM_001396040.1:c.*2816G= NP_001382969.1:n.*2816G=
NM_001396041.1:c.813+5405G= NP_001382970.1:n.813+5405G=
NM_001396042.1:c.690+9960G= NP_001382971.1:n.690+9960G=
NM_001396043.1:c.813+5405G= NP_001382972.1:n.813+5405G=
NM_001396044.1:c.813+5405G= NP_001382973.1:n.813+5405G=
NM_001396045.1:c.690+9960G= NP_001382974.1:n.690+9960G=
NR_173242.1:n.3798G=