Canonical Allele Identifier: CA4783961

Gene: TMEM70

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.73976434C>T , CM000670.2:g.73976434C>T	GRCh38
NC_000008.10:g.74888669C>T , CM000670.1:g.74888669C>T	GRCh37
NC_000008.9:g.75051223C>T	NCBI36
NG_016618.1:g.5293C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_017866.6:c.153C>T MANE Select	NP_060336.3:p.Gly51=
ENST00000312184.6:c.153C>T MANE Select	ENSP00000312599.5:p.Gly51=
NM_001040613.2:c.153C>T	NP_001035703.1:p.Gly51=
NM_001040613.3:c.153C>T	NP_001035703.1:p.Gly51=
NM_017866.5:c.153C>T	NP_060336.3:p.Gly51=
NR_033334.1:n.293C>T
NR_033334.2:n.240C>T
ENST00000312184.5:c.153C>T	ENSP00000312599.5:p.Gly51=
ENST00000416961.6:c.153C>T	ENSP00000407695.2:p.Gly51=
ENST00000517439.1:c.153C>T	ENSP00000429467.1:p.Gly51=
ENST00000517614.1:n.216C>T
ENST00000520167.5:n.317+473C>T
ENST00000523794.1:n.704C>T