Canonical Allele Identifier: CA2693446569

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38675971-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675971G>A , CM000685.2:g.38675971G>A	GRCh38
NC_000023.10:g.38535225G>A , CM000685.1:g.38535225G>A	GRCh37
NC_000023.9:g.38420169G>A	NCBI36
NG_009160.1:g.119495G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+111G>A MANE Select	ENSP00000367743.2:n.597+111G>A
ENST00000286824.6:c.648+111G>A	ENSP00000286824.6:n.648+111G>A
ENST00000378482.6:c.597+111G>A	ENSP00000367743.2:n.597+111G>A
ENST00000419600.3:n.541+111G>A
ENST00000465127.1:c.687+111G>A	ENSP00000417050.1:n.687+111G>A
ENST00000471410.5:c.*623+111G>A	ENSP00000419290.1:n.*623+111G>A
ENST00000475216.5:c.*590+111G>A	ENSP00000418586.1:n.*590+111G>A
NM_004615.3:c.597+111G>A	NP_004606.2:n.597+111G>A
NM_004615.4:c.597+111G>A MANE Select	NP_004606.2:n.597+111G>A