Canonical Allele Identifier: CA2693446580

Gene: TSPAN7

Linked Data

• gnomAD v4: X-38676000-T-TCTCCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38676000_38676001insCTCCCA , CM000685.2:g.38676000_38676001insCTCCCA	GRCh38
NC_000023.10:g.38535254_38535255insCTCCCA , CM000685.1:g.38535254_38535255insCTCCCA	GRCh37
NC_000023.9:g.38420198_38420199insCTCCCA	NCBI36
NG_009160.1:g.119524_119525insCTCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.597+140_597+141insCTCCCA MANE Select	ENSP00000367743.2:n.597+140_597+141insCTCCCA
ENST00000286824.6:c.648+140_648+141insCTCCCA	ENSP00000286824.6:n.648+140_648+141insCTCCCA
ENST00000378482.6:c.597+140_597+141insCTCCCA	ENSP00000367743.2:n.597+140_597+141insCTCCCA
ENST00000419600.3:n.541+140_541+141insCTCCCA
ENST00000465127.1:c.687+140_687+141insCTCCCA	ENSP00000417050.1:n.687+140_687+141insCTCCCA
ENST00000471410.5:c.*623+140_*623+141insCTCCCA	ENSP00000419290.1:n.*623+140_*623+141insCTCCCA
ENST00000475216.5:c.*590+140_*590+141insCTCCCA	ENSP00000418586.1:n.*590+140_*590+141insCTCCCA
NM_004615.3:c.597+140_597+141insCTCCCA	NP_004606.2:n.597+140_597+141insCTCCCA
NM_004615.4:c.597+140_597+141insCTCCCA MANE Select	NP_004606.2:n.597+140_597+141insCTCCCA