Canonical Allele Identifier: CA412982273

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38535058T>C (hg19) ; chrX:g.38675804T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675804T>C , CM000685.2:g.38675804T>C	GRCh38
NC_000023.10:g.38535058T>C , CM000685.1:g.38535058T>C	GRCh37
NC_000023.9:g.38420002T>C	NCBI36
NG_009160.1:g.119328T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.541T>C MANE Select	ENSP00000367743.2:p.Cys181Arg
ENST00000286824.6:c.592T>C	ENSP00000286824.6:p.Cys198Arg
ENST00000378482.6:c.541T>C	ENSP00000367743.2:p.Cys181Arg
ENST00000419600.3:n.485T>C
ENST00000465127.1:c.631T>C	ENSP00000417050.1:p.Cys211Arg
ENST00000471410.5:c.*567T>C	ENSP00000419290.1:n.*567T>C
ENST00000475216.5:c.*534T>C	ENSP00000418586.1:n.*534T>C
ENST00000488893.5:n.724T>C
NM_004615.3:c.541T>C	NP_004606.2:p.Cys181Arg
NM_004615.4:c.541T>C MANE Select	NP_004606.2:p.Cys181Arg