Canonical Allele Identifier: CA1793942820

Gene: TMEM70

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.73976409G= , CM000670.2:g.73976409G=	GRCh38
NC_000008.10:g.74888644G= , CM000670.1:g.74888644G=	GRCh37
NC_000008.9:g.75051198G=	NCBI36
NG_016618.1:g.5268G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000312184.6:c.128G= MANE Select	ENSP00000312599.5:p.Ser43=
ENST00000312184.5:c.128G=	ENSP00000312599.5:p.Ser43=
ENST00000416961.6:c.128G=	ENSP00000407695.2:p.Ser43=
ENST00000517439.1:c.128G=	ENSP00000429467.1:p.Ser43=
ENST00000517614.1:n.191G=
ENST00000520167.5:n.317+448G=
ENST00000523794.1:n.679G=
NM_001040613.2:c.128G=	NP_001035703.1:p.Ser43=
NM_017866.5:c.128G=	NP_060336.3:p.Ser43=
NR_033334.1:n.268G=
NM_017866.6:c.128G= MANE Select	NP_060336.3:p.Ser43=
NM_001040613.3:c.128G=	NP_001035703.1:p.Ser43=
NR_033334.2:n.215G=