Canonical Allele Identifier: CA515685032

Gene: TSPAN7

Linked Data

• MyVariant Identifiers: chrX:g.38534964C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675710C>T , CM000685.2:g.38675710C>T	GRCh38
NC_000023.10:g.38534964C>T , CM000685.1:g.38534964C>T	GRCh37
NC_000023.9:g.38419908C>T	NCBI36
NG_009160.1:g.119234C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378482.7:c.447C>T MANE Select	ENSP00000367743.2:p.Ser149=
ENST00000286824.6:c.498C>T	ENSP00000286824.6:p.Ser166=
ENST00000378482.6:c.447C>T	ENSP00000367743.2:p.Ser149=
ENST00000419600.3:n.391C>T
ENST00000465127.1:c.537C>T	ENSP00000417050.1:p.Ser179=
ENST00000471410.5:c.*473C>T	ENSP00000419290.1:n.*473C>T
ENST00000475216.5:c.*440C>T	ENSP00000418586.1:n.*440C>T
ENST00000488893.5:n.630C>T
NM_004615.3:c.447C>T	NP_004606.2:p.Ser149=
NM_004615.4:c.447C>T MANE Select	NP_004606.2:p.Ser149=