Canonical Allele Identifier: CA1793942813

Gene: TMEM70

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.73976401C= , CM000670.2:g.73976401C=	GRCh38
NC_000008.10:g.74888636C= , CM000670.1:g.74888636C=	GRCh37
NC_000008.9:g.75051190C=	NCBI36
NG_016618.1:g.5260C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312184.6:c.120C= MANE Select	ENSP00000312599.5:p.Ser40=
ENST00000312184.5:c.120C=	ENSP00000312599.5:p.Ser40=
ENST00000416961.6:c.120C=	ENSP00000407695.2:p.Ser40=
ENST00000517439.1:c.120C=	ENSP00000429467.1:p.Ser40=
ENST00000517614.1:n.183C=
ENST00000520167.5:n.317+440C=
ENST00000523794.1:n.671C=
NM_001040613.2:c.120C=	NP_001035703.1:p.Ser40=
NM_017866.5:c.120C=	NP_060336.3:p.Ser40=
NR_033334.1:n.260C=
NM_017866.6:c.120C= MANE Select	NP_060336.3:p.Ser40=
NM_001040613.3:c.120C=	NP_001035703.1:p.Ser40=
NR_033334.2:n.207C=