Canonical Allele Identifier: CA209249467

Gene: TSPAN15

Linked Data

• dbSNP Id: rs985103629
• gnomAD v2: 10-71218030-G-A
• gnomAD v3: 10-69458274-G-A
• gnomAD v4: 10-69458274-G-A
• MyVariant Identifiers: chr10:g.71218030G>A (hg19) ; chr10:g.69458274G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69458274G>A , CM000672.2:g.69458274G>A	GRCh38
NC_000010.10:g.71218030G>A , CM000672.1:g.71218030G>A	GRCh37
NC_000010.9:g.70888036G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373290.7:c.96+6584G>A MANE Select	ENSP00000362387.2:n.96+6584G>A
ENST00000373290.6:c.96+6584G>A	ENSP00000362387.2:n.96+6584G>A
ENST00000478112.1:n.214+6584G>A
NM_012339.3:c.96+6584G>A	NP_036471.1:n.96+6584G>A
XM_005269667.3:c.96+6584G>A	XP_005269724.1:n.96+6584G>A
XM_006717738.2:c.25-25417G>A	XP_006717801.1:n.25-25417G>A
XR_945642.1:n.226+6584G>A
NM_001351263.1:c.96+6584G>A	NP_001338192.1:n.96+6584G>A
NM_012339.4:c.96+6584G>A	NP_036471.1:n.96+6584G>A
NR_147091.1:n.224+6584G>A
XM_017016010.1:c.96+6584G>A	XP_016871499.1:n.96+6584G>A
XR_001747072.1:n.227+6584G>A
XR_001747073.1:n.227+6584G>A
XR_001747074.1:n.224+6584G>A
NM_012339.5:c.96+6584G>A MANE Select	NP_036471.1:n.96+6584G>A
NM_001351263.2:c.96+6584G>A	NP_001338192.1:n.96+6584G>A
NR_147091.2:n.226+6584G>A