Canonical Allele Identifier: CA1132427442

Gene: TSPAN7

Linked Data

• gnomAD v3: X-38675789-A-ATTTT
• gnomAD v4: X-38675789-A-ATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675790_38675791insTTTT , CM000685.2:g.38675790_38675791insTTTT	GRCh38
NC_000023.10:g.38535044_38535045insTTTT , CM000685.1:g.38535044_38535045insTTTT	GRCh37
NC_000023.9:g.38419988_38419989insTTTT	NCBI36
NG_009160.1:g.119314_119315insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.527_528insTTTT MANE Select	ENSP00000367743.2:p.Met176IlefsTer6
ENST00000286824.6:c.578_579insTTTT	ENSP00000286824.6:p.Met193IlefsTer6
ENST00000378482.6:c.527_528insTTTT	ENSP00000367743.2:p.Met176IlefsTer6
ENST00000419600.3:n.471_472insTTTT
ENST00000465127.1:c.617_618insTTTT	ENSP00000417050.1:p.Met206IlefsTer6
ENST00000471410.5:c.*553_*554insTTTT	ENSP00000419290.1:n.*553_*554insTTTT
ENST00000475216.5:c.*520_*521insTTTT	ENSP00000418586.1:n.*520_*521insTTTT
ENST00000488893.5:n.710_711insTTTT
NM_004615.3:c.527_528insTTTT	NP_004606.2:p.Met176IlefsTer6
NM_004615.4:c.527_528insTTTT MANE Select	NP_004606.2:p.Met176IlefsTer6