Canonical Allele Identifier: CA1839089484

Gene: MTAP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21816743A= , CM000671.2:g.21816743A=	GRCh38
NC_000009.11:g.21816742A= , CM000671.1:g.21816742A=	GRCh37
NC_000009.10:g.21806742A=	NCBI36
NG_032650.1:g.19108A=
NG_032650.2:g.19108A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404796.3:c.150A=	ENSP00000385916.2:p.Ile50=
ENST00000644715.2:c.150A= MANE Select	ENSP00000494373.1:p.Ile50=
ENST00000380172.8:c.150A=	ENSP00000369519.4:p.Ile50=
ENST00000404796.2:c.150A=	ENSP00000385916.2:p.Ile50=
ENST00000419385.5:c.*22A=	ENSP00000393507.1:n.*22A=
ENST00000427788.2:n.536A=
ENST00000460874.6:c.201A=	ENSP00000461932.1:p.Ile67=
ENST00000579422.5:n.538A=
ENST00000580718.1:c.150A=	ENSP00000464616.1:p.Ile50=
ENST00000580900.5:c.150A=	ENSP00000463424.1:p.Ile50=
NM_002451.3:c.150A=	NP_002442.2:p.Ile50=
NM_002451.4:c.150A= MANE Select	NP_002442.2:p.Ile50=
NM_001396040.1:c.201A=	NP_001382969.1:p.Ile67=
NM_001396041.1:c.150A=	NP_001382970.1:p.Ile50=
NM_001396042.1:c.150A=	NP_001382971.1:p.Ile50=
NM_001396043.1:c.150A=	NP_001382972.1:p.Ile50=
NM_001396044.1:c.150A=	NP_001382973.1:p.Ile50=
NM_001396045.1:c.150A=	NP_001382974.1:p.Ile50=
NR_173242.1:n.263A=