Canonical Allele Identifier: CA1793942818

Gene: TMEM70

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.73976407C= , CM000670.2:g.73976407C=	GRCh38
NC_000008.10:g.74888642C= , CM000670.1:g.74888642C=	GRCh37
NC_000008.9:g.75051196C=	NCBI36
NG_016618.1:g.5266C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000312184.6:c.126C= MANE Select	ENSP00000312599.5:p.Ser42=
ENST00000312184.5:c.126C=	ENSP00000312599.5:p.Ser42=
ENST00000416961.6:c.126C=	ENSP00000407695.2:p.Ser42=
ENST00000517439.1:c.126C=	ENSP00000429467.1:p.Ser42=
ENST00000517614.1:n.189C=
ENST00000520167.5:n.317+446C=
ENST00000523794.1:n.677C=
NM_001040613.2:c.126C=	NP_001035703.1:p.Ser42=
NM_017866.5:c.126C=	NP_060336.3:p.Ser42=
NR_033334.1:n.266C=
NM_017866.6:c.126C= MANE Select	NP_060336.3:p.Ser42=
NM_001040613.3:c.126C=	NP_001035703.1:p.Ser42=
NR_033334.2:n.213C=