Canonical Allele Identifier: CA1793942758

Gene: TMEM70

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.73976308G= , CM000670.2:g.73976308G=	GRCh38
NC_000008.10:g.74888543G= , CM000670.1:g.74888543G=	GRCh37
NC_000008.9:g.75051097G=	NCBI36
NG_016618.1:g.5167G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000312184.6:c.27G= MANE Select	ENSP00000312599.5:p.Pro9=
ENST00000312184.5:c.27G=	ENSP00000312599.5:p.Pro9=
ENST00000416961.6:c.27G=	ENSP00000407695.2:p.Pro9=
ENST00000517439.1:c.27G=	ENSP00000429467.1:p.Pro9=
ENST00000517614.1:n.90G=
ENST00000520167.5:n.317+347G=
ENST00000523794.1:n.578G=
NM_001040613.2:c.27G=	NP_001035703.1:p.Pro9=
NM_017866.5:c.27G=	NP_060336.3:p.Pro9=
NR_033334.1:n.167G=
NM_017866.6:c.27G= MANE Select	NP_060336.3:p.Pro9=
NM_001040613.3:c.27G=	NP_001035703.1:p.Pro9=
NR_033334.2:n.114G=