Canonical Allele Identifier: CA1839116420

Gene: MTAP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21864845_21864848delinsCTCT , CM000671.2:g.21864845_21864848delinsCTCT	GRCh38
NC_000009.11:g.21864844_21864847delinsCTCT , CM000671.1:g.21864844_21864847delinsCTCT	GRCh37
NC_000009.10:g.21854844_21854847delinsCTCT	NCBI36
NG_032650.1:g.67210_67213delinsCTCT
NG_032650.2:g.67210_67213delinsCTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000404796.3:c.347+46643_347+46646delinsCTCT	ENSP00000385916.2:n.347+46643_347+46646de...
ENST00000644715.2:c.*2831_*2834delinsCTCT MANE Select	ENSP00000494373.1:n.*2831_*2834delinsCTCT...
ENST00000380172.8:c.*2831_*2834delinsCTCT	ENSP00000369519.4:n.*2831_*2834delinsCTCT...
ENST00000404796.2:c.347+46643_347+46646delinsCTCT	ENSP00000385916.2:n.347+46643_347+46646de...
ENST00000577563.1:c.147+9975_147+9978delinsCTCT	ENSP00000462082.1:n.147+9975_147+9978deli...
ENST00000580900.5:c.813+5420_813+5423delinsCTCT	ENSP00000463424.1:n.813+5420_813+5423deli...
NM_002451.3:c.*2831_*2834delinsCTCT	NP_002442.2:n.*2831_*2834delinsCTCT
NM_002451.4:c.*2831_*2834delinsCTCT MANE Select	NP_002442.2:n.*2831_*2834delinsCTCT
NM_001396040.1:c.*2831_*2834delinsCTCT	NP_001382969.1:n.*2831_*2834delinsCTCT
NM_001396041.1:c.813+5420_813+5423delinsCTCT	NP_001382970.1:n.813+5420_813+5423delinsC...
NM_001396042.1:c.690+9975_690+9978delinsCTCT	NP_001382971.1:n.690+9975_690+9978delinsC...
NM_001396043.1:c.813+5420_813+5423delinsCTCT	NP_001382972.1:n.813+5420_813+5423delinsC...
NM_001396044.1:c.813+5420_813+5423delinsCTCT	NP_001382973.1:n.813+5420_813+5423delinsC...
NM_001396045.1:c.690+9975_690+9978delinsCTCT	NP_001382974.1:n.690+9975_690+9978delinsC...
NR_173242.1:n.3813_3816delinsCTCT