Canonical Allele Identifier: CA2689593174

Gene: MTAP

Linked Data

• gnomAD v4: 9-21864827-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21864827A>C , CM000671.2:g.21864827A>C	GRCh38
NC_000009.11:g.21864826A>C , CM000671.1:g.21864826A>C	GRCh37
NC_000009.10:g.21854826A>C	NCBI36
NG_032650.1:g.67192A>C
NG_032650.2:g.67192A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000404796.3:c.347+46625A>C	ENSP00000385916.2:n.347+46625A>C
ENST00000644715.2:c.*2813A>C MANE Select	ENSP00000494373.1:n.*2813A>C
ENST00000380172.8:c.*2813A>C	ENSP00000369519.4:n.*2813A>C
ENST00000404796.2:c.347+46625A>C	ENSP00000385916.2:n.347+46625A>C
ENST00000577563.1:c.147+9957A>C	ENSP00000462082.1:n.147+9957A>C
ENST00000580900.5:c.813+5402A>C	ENSP00000463424.1:n.813+5402A>C
NM_002451.3:c.*2813A>C	NP_002442.2:n.*2813A>C
NM_002451.4:c.*2813A>C MANE Select	NP_002442.2:n.*2813A>C
NM_001396040.1:c.*2813A>C	NP_001382969.1:n.*2813A>C
NM_001396041.1:c.813+5402A>C	NP_001382970.1:n.813+5402A>C
NM_001396042.1:c.690+9957A>C	NP_001382971.1:n.690+9957A>C
NM_001396043.1:c.813+5402A>C	NP_001382972.1:n.813+5402A>C
NM_001396044.1:c.813+5402A>C	NP_001382973.1:n.813+5402A>C
NM_001396045.1:c.690+9957A>C	NP_001382974.1:n.690+9957A>C
NR_173242.1:n.3795A>C