Canonical Allele Identifier: CA2693446584

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38676001-G-GGCAATCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38676002_38676003insCAATCAAG , CM000685.2:g.38676002_38676003insCAATCAAG	GRCh38
NC_000023.10:g.38535256_38535257insCAATCAAG , CM000685.1:g.38535256_38535257insCAATCAAG	GRCh37
NC_000023.9:g.38420200_38420201insCAATCAAG	NCBI36
NG_009160.1:g.119526_119527insCAATCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+142_597+143insCAATCAAG MANE Select	ENSP00000367743.2:n.597+142_597+143insCAATCAAG
ENST00000286824.6:c.648+142_648+143insCAATCAAG	ENSP00000286824.6:n.648+142_648+143insCAATCAAG
ENST00000378482.6:c.597+142_597+143insCAATCAAG	ENSP00000367743.2:n.597+142_597+143insCAATCAAG
ENST00000419600.3:n.541+142_541+143insCAATCAAG
ENST00000465127.1:c.687+142_687+143insCAATCAAG	ENSP00000417050.1:n.687+142_687+143insCAATCAAG
ENST00000471410.5:c.*623+142_*623+143insCAATCAAG	ENSP00000419290.1:n.*623+142_*623+143insCAATCAAG
ENST00000475216.5:c.*590+142_*590+143insCAATCAAG	ENSP00000418586.1:n.*590+142_*590+143insCAATCAAG
NM_004615.3:c.597+142_597+143insCAATCAAG	NP_004606.2:n.597+142_597+143insCAATCAAG
NM_004615.4:c.597+142_597+143insCAATCAAG MANE Select	NP_004606.2:n.597+142_597+143insCAATCAAG