Canonical Allele Identifier: CA412982394
Gene: TSPAN7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.38535113A>C (hg19) chrX:g.38675859A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.38675859A>C , CM000685.2:g.38675859A>C GRCh38
NC_000023.10:g.38535113A>C , CM000685.1:g.38535113A>C GRCh37
NC_000023.9:g.38420057A>C NCBI36
NG_009160.1:g.119383A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378482.7:c.596A>C MANE Select ENSP00000367743.2:p.Lys199Thr
ENST00000286824.6:c.647A>C ENSP00000286824.6:p.Lys216Thr
ENST00000378482.6:c.596A>C ENSP00000367743.2:p.Lys199Thr
ENST00000419600.3:n.540A>C
ENST00000465127.1:c.686A>C ENSP00000417050.1:p.Lys229Thr
ENST00000471410.5:c.*622A>C ENSP00000419290.1:n.*622A>C
ENST00000475216.5:c.*589A>C ENSP00000418586.1:n.*589A>C
NM_004615.3:c.596A>C NP_004606.2:p.Lys199Thr
NM_004615.4:c.596A>C MANE Select NP_004606.2:p.Lys199Thr
Search 100 bp 5'
Search 100 bp 3'