Canonical Allele Identifier: CA2693446582

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38676000-TGGGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38676001_38676005del , CM000685.2:g.38676001_38676005del	GRCh38
NC_000023.10:g.38535255_38535259del , CM000685.1:g.38535255_38535259del	GRCh37
NC_000023.9:g.38420199_38420203del	NCBI36
NG_009160.1:g.119525_119529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+141_597+145del MANE Select	ENSP00000367743.2:n.597+141_597+145del
ENST00000286824.6:c.648+141_648+145del	ENSP00000286824.6:n.648+141_648+145del
ENST00000378482.6:c.597+141_597+145del	ENSP00000367743.2:n.597+141_597+145del
ENST00000419600.3:n.541+141_541+145del
ENST00000465127.1:c.687+141_687+145del	ENSP00000417050.1:n.687+141_687+145del
ENST00000471410.5:c.*623+141_*623+145del	ENSP00000419290.1:n.*623+141_*623+145del
ENST00000475216.5:c.*590+141_*590+145del	ENSP00000418586.1:n.*590+141_*590+145del
NM_004615.3:c.597+141_597+145del	NP_004606.2:n.597+141_597+145del
NM_004615.4:c.597+141_597+145del MANE Select	NP_004606.2:n.597+141_597+145del