Canonical Allele Identifier: CA1132427510
Gene: TSPAN7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675814_38675815insCC , CM000685.2:g.38675814_38675815insCC GRCh38
NC_000023.10:g.38535068_38535069insCC , CM000685.1:g.38535068_38535069insCC GRCh37
NC_000023.9:g.38420012_38420013insCC NCBI36
NG_009160.1:g.119338_119339insCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.551_552insCC MANE Select ENSP00000367743.2:p.Gln184HisfsTer7
ENST00000286824.6:c.602_603insCC ENSP00000286824.6:p.Gln201HisfsTer7
ENST00000378482.6:c.551_552insCC ENSP00000367743.2:p.Gln184HisfsTer7
ENST00000419600.3:n.495_496insCC
ENST00000465127.1:c.641_642insCC ENSP00000417050.1:p.Gln214HisfsTer7
ENST00000471410.5:c.*577_*578insCC ENSP00000419290.1:n.*577_*578insCC
ENST00000475216.5:c.*544_*545insCC ENSP00000418586.1:n.*544_*545insCC
ENST00000488893.5:n.734_735insCC
NM_004615.3:c.551_552insCC NP_004606.2:p.Gln184HisfsTer7
NM_004615.4:c.551_552insCC MANE Select NP_004606.2:p.Gln184HisfsTer7