Canonical Allele Identifier: CA209249429

Gene: TSPAN15

Linked Data

• dbSNP Id: rs34338896
• gnomAD v2: 10-71218012-C-CAGG
• gnomAD v3: 10-69458256-C-CAGG
• gnomAD v4: 10-69458256-C-CAGG
• MyVariant Identifiers: chr10:g.71218012_71218013insAGG (hg19) ; chr10:g.69458256_69458257insAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69458259_69458261dup , CM000672.2:g.69458259_69458261dup	GRCh38
NC_000010.10:g.71218015_71218017dup , CM000672.1:g.71218015_71218017dup	GRCh37
NC_000010.9:g.70888021_70888023dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.96+6569_96+6571dup MANE Select	ENSP00000362387.2:n.96+6569_96+6571dup
ENST00000373290.6:c.96+6569_96+6571dup	ENSP00000362387.2:n.96+6569_96+6571dup
ENST00000478112.1:n.214+6569_214+6571dup
NM_012339.3:c.96+6569_96+6571dup	NP_036471.1:n.96+6569_96+6571dup
XM_005269667.3:c.96+6569_96+6571dup	XP_005269724.1:n.96+6569_96+6571dup
XM_006717738.2:c.25-25432_25-25430dup	XP_006717801.1:n.25-25432_25-25430dup
XR_945642.1:n.226+6569_226+6571dup
NM_001351263.1:c.96+6569_96+6571dup	NP_001338192.1:n.96+6569_96+6571dup
NM_012339.4:c.96+6569_96+6571dup	NP_036471.1:n.96+6569_96+6571dup
NR_147091.1:n.224+6569_224+6571dup
XM_017016010.1:c.96+6569_96+6571dup	XP_016871499.1:n.96+6569_96+6571dup
XR_001747072.1:n.227+6569_227+6571dup
XR_001747073.1:n.227+6569_227+6571dup
XR_001747074.1:n.224+6569_224+6571dup
NM_012339.5:c.96+6569_96+6571dup MANE Select	NP_036471.1:n.96+6569_96+6571dup
NM_001351263.2:c.96+6569_96+6571dup	NP_001338192.1:n.96+6569_96+6571dup
NR_147091.2:n.226+6569_226+6571dup