Canonical Allele Identifier: CA2693446543

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38675913-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675919dup , CM000685.2:g.38675919dup	GRCh38
NC_000023.10:g.38535173dup , CM000685.1:g.38535173dup	GRCh37
NC_000023.9:g.38420117dup	NCBI36
NG_009160.1:g.119443dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+59dup MANE Select	ENSP00000367743.2:n.597+59dup
ENST00000286824.6:c.648+59dup	ENSP00000286824.6:n.648+59dup
ENST00000378482.6:c.597+59dup	ENSP00000367743.2:n.597+59dup
ENST00000419600.3:n.541+59dup
ENST00000465127.1:c.687+59dup	ENSP00000417050.1:n.687+59dup
ENST00000471410.5:c.*623+59dup	ENSP00000419290.1:n.*623+59dup
ENST00000475216.5:c.*590+59dup	ENSP00000418586.1:n.*590+59dup
NM_004615.3:c.597+59dup	NP_004606.2:n.597+59dup
NM_004615.4:c.597+59dup MANE Select	NP_004606.2:n.597+59dup