Canonical Allele Identifier: CA6112657
Gene: TSGA10IP HGNC NCBI

Linked Data

dbSNP Id: rs71455793

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000532620.6:c.908G>A MANE Select ENSP00000484252.1:p.Arg303Gln
ENST00000532620.5:c.908G>A ENSP00000484252.1:p.Arg303Gln
ENST00000534740.5:c.147+1911G>A ENSP00000482640.1:n.147+1911G>A
ENST00000608857.2:c.908G>A ENSP00000477317.2:p.Arg303Gln
NM_152762.2:c.908G>A NP_689975.2:p.Arg303Gln
XM_011544887.1:c.908G>A XP_011543189.1:p.Arg303Gln
XM_011544888.1:c.500G>A XP_011543190.1:p.Arg167Gln
XR_949858.1:n.1139G>A
XM_011544887.2:c.908G>A XP_011543189.1:p.Arg303Gln
XM_011544888.2:c.500G>A XP_011543190.1:p.Arg167Gln
NM_001395491.1:c.908G>A NP_001382420.1:p.Arg303Gln
NM_001395492.1:c.500G>A NP_001382421.1:p.Arg167Gln
NM_001395493.1:c.500G>A NP_001382422.1:p.Arg167Gln
NM_001395494.1:c.148-312G>A NP_001382423.1:n.148-312G>A
NM_001395495.1:c.119-268G>A NP_001382424.1:n.119-268G>A
NM_152762.3:c.908G>A MANE Select NP_689975.2:p.Arg303Gln
NR_172563.1:n.343+1911G>A