Canonical Allele Identifier: CA875199917

Gene: TSPAN7

Linked Data

• dbSNP Id: rs1489776518
• gnomAD v3: X-38675624-T-TTA
• gnomAD v4: X-38675624-T-TTA
• MyVariant Identifiers: chrX:g.38534878_38534879insTA (hg19) ; chrX:g.38675624_38675625insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.38675627_38675628dup , CM000685.2:g.38675627_38675628dup	GRCh38
NC_000023.10:g.38534881_38534882dup , CM000685.1:g.38534881_38534882dup	GRCh37
NC_000023.9:g.38419825_38419826dup	NCBI36
NG_009160.1:g.119151_119152dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378482.7:c.442-78_442-77dup MANE Select	ENSP00000367743.2:n.442-78_442-77dup
ENST00000286824.6:c.493-78_493-77dup	ENSP00000286824.6:n.493-78_493-77dup
ENST00000378482.6:c.442-78_442-77dup	ENSP00000367743.2:n.442-78_442-77dup
ENST00000419600.3:n.386-78_386-77dup
ENST00000465127.1:c.532-78_532-77dup	ENSP00000417050.1:n.532-78_532-77dup
ENST00000471410.5:c.*468-78_*468-77dup	ENSP00000419290.1:n.*468-78_*468-77dup
ENST00000475216.5:c.*435-78_*435-77dup	ENSP00000418586.1:n.*435-78_*435-77dup
ENST00000488893.5:n.625-78_625-77dup
NM_004615.3:c.442-78_442-77dup	NP_004606.2:n.442-78_442-77dup
NM_004615.4:c.442-78_442-77dup MANE Select	NP_004606.2:n.442-78_442-77dup