Canonical Allele Identifier: CA1132427515
Gene: TSPAN7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675815_38675816insA , CM000685.2:g.38675815_38675816insA GRCh38
NC_000023.10:g.38535069_38535070insA , CM000685.1:g.38535069_38535070insA GRCh37
NC_000023.9:g.38420013_38420014insA NCBI36
NG_009160.1:g.119339_119340insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.552_553insA MANE Select ENSP00000367743.2:p.Asp185ArgfsTer13
ENST00000286824.6:c.603_604insA ENSP00000286824.6:p.Asp202ArgfsTer13
ENST00000378482.6:c.552_553insA ENSP00000367743.2:p.Asp185ArgfsTer13
ENST00000419600.3:n.496_497insA
ENST00000465127.1:c.642_643insA ENSP00000417050.1:p.Asp215ArgfsTer13
ENST00000471410.5:c.*578_*579insA ENSP00000419290.1:n.*578_*579insA
ENST00000475216.5:c.*545_*546insA ENSP00000418586.1:n.*545_*546insA
ENST00000488893.5:n.735_736insA
NM_004615.3:c.552_553insA NP_004606.2:p.Asp185ArgfsTer13
NM_004615.4:c.552_553insA MANE Select NP_004606.2:p.Asp185ArgfsTer13