Canonical Allele Identifier: CA515685486
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38535084G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675830G>C , CM000685.2:g.38675830G>C GRCh38
NC_000023.10:g.38535084G>C , CM000685.1:g.38535084G>C GRCh37
NC_000023.9:g.38420028G>C NCBI36
NG_009160.1:g.119354G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.567G>C MANE Select ENSP00000367743.2:p.Leu189=
ENST00000286824.6:c.618G>C ENSP00000286824.6:p.Leu206=
ENST00000378482.6:c.567G>C ENSP00000367743.2:p.Leu189=
ENST00000419600.3:n.511G>C
ENST00000465127.1:c.657G>C ENSP00000417050.1:p.Leu219=
ENST00000471410.5:c.*593G>C ENSP00000419290.1:n.*593G>C
ENST00000475216.5:c.*560G>C ENSP00000418586.1:n.*560G>C
NM_004615.3:c.567G>C NP_004606.2:p.Leu189=
NM_004615.4:c.567G>C MANE Select NP_004606.2:p.Leu189=
Search 100 bp 5'
Search 100 bp 3'