Canonical Allele Identifier: CA2579585179

Gene: TSPAN7

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675929A>C , CM000685.2:g.38675929A>C	GRCh38
NC_000023.10:g.38535183A>C , CM000685.1:g.38535183A>C	GRCh37
NC_000023.9:g.38420127A>C	NCBI36
NG_009160.1:g.119453A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+69A>C MANE Select	ENSP00000367743.2:n.597+69A>C
ENST00000286824.6:c.648+69A>C	ENSP00000286824.6:n.648+69A>C
ENST00000378482.6:c.597+69A>C	ENSP00000367743.2:n.597+69A>C
ENST00000419600.3:n.541+69A>C
ENST00000465127.1:c.687+69A>C	ENSP00000417050.1:n.687+69A>C
ENST00000471410.5:c.*623+69A>C	ENSP00000419290.1:n.*623+69A>C
ENST00000475216.5:c.*590+69A>C	ENSP00000418586.1:n.*590+69A>C
NM_004615.3:c.597+69A>C	NP_004606.2:n.597+69A>C
NM_004615.4:c.597+69A>C MANE Select	NP_004606.2:n.597+69A>C