Canonical Allele Identifier: CA1132427371

Gene: TSPAN7

Linked Data

• dbSNP Id: rs2069847629
• gnomAD v3: X-38675533-T-TCAAACATTTC
• gnomAD v4: X-38675533-T-TCAAACATTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675536_38675537insACATTTCCAA , CM000685.2:g.38675536_38675537insACATTTCCAA	GRCh38
NC_000023.10:g.38534790_38534791insACATTTCCAA , CM000685.1:g.38534790_38534791insACATTTCCAA	GRCh37
NC_000023.9:g.38419734_38419735insACATTTCCAA	NCBI36
NG_009160.1:g.119060_119061insACATTTCCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.442-169_442-168insACATTTCCAA MANE Select	ENSP00000367743.2:n.442-169_442-168insACATTTCCAA
ENST00000286824.6:c.493-169_493-168insACATTTCCAA	ENSP00000286824.6:n.493-169_493-168insACATTTCCAA
ENST00000378482.6:c.442-169_442-168insACATTTCCAA	ENSP00000367743.2:n.442-169_442-168insACATTTCCAA
ENST00000419600.3:n.386-169_386-168insACATTTCCAA
ENST00000465127.1:c.532-169_532-168insACATTTCCAA	ENSP00000417050.1:n.532-169_532-168insACATTTCCAA
ENST00000471410.5:c.*468-169_*468-168insACATTTCCAA	ENSP00000419290.1:n.*468-169_*468-168insACATTTCCAA
ENST00000475216.5:c.*435-169_*435-168insACATTTCCAA	ENSP00000418586.1:n.*435-169_*435-168insACATTTCCAA
ENST00000488893.5:n.625-169_625-168insACATTTCCAA
NM_004615.3:c.442-169_442-168insACATTTCCAA	NP_004606.2:n.442-169_442-168insACATTTCCAA
NM_004615.4:c.442-169_442-168insACATTTCCAA MANE Select	NP_004606.2:n.442-169_442-168insACATTTCCAA