Canonical Allele Identifier: CA1979476467

Gene: TSGA10IP

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65947733G= , CM000673.2:g.65947733G=	GRCh38
NC_000011.9:g.65715204G= , CM000673.1:g.65715204G=	GRCh37
NC_000011.8:g.65471780G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_152762.3:c.908G= MANE Select	NP_689975.2:p.Arg303=
ENST00000532620.6:c.908G= MANE Select	ENSP00000484252.1:p.Arg303=
NM_001395491.1:c.908G=	NP_001382420.1:p.Arg303=
NM_001395492.1:c.500G=	NP_001382421.1:p.Arg167=
NM_001395493.1:c.500G=	NP_001382422.1:p.Arg167=
NM_001395494.1:c.148-312G=	NP_001382423.1:n.148-312G=
NM_001395495.1:c.119-268G=	NP_001382424.1:n.119-268G=
NM_152762.2:c.908G=	NP_689975.2:p.Arg303=
NR_172563.1:n.343+1911G=
ENST00000532620.5:c.908G=	ENSP00000484252.1:p.Arg303=
ENST00000534740.5:c.147+1911G=	ENSP00000482640.1:n.147+1911G=
ENST00000608857.2:c.908G=	ENSP00000477317.2:p.Arg303=
XM_011544887.1:c.908G=	XP_011543189.1:p.Arg303=
XM_011544887.2:c.908G=	XP_011543189.1:p.Arg303=
XM_011544888.1:c.500G=	XP_011543190.1:p.Arg167=
XM_011544888.2:c.500G=	XP_011543190.1:p.Arg167=
XR_949858.1:n.1139G=