Canonical Allele Identifier: CA2722294510

Gene: TSPAN15

Linked Data

• dbSNP Id: rs2133116432

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485476G>A , CM000672.2:g.69485476G>A	GRCh38
NC_000010.10:g.71245232G>A , CM000672.1:g.71245232G>A	GRCh37
NC_000010.9:g.70915238G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373290.7:c.357+261G>A MANE Select	ENSP00000362387.2:n.357+261G>A
ENST00000373290.6:c.357+261G>A	ENSP00000362387.2:n.357+261G>A
ENST00000452130.1:c.84+261G>A	ENSP00000404528.1:n.84+261G>A
ENST00000475069.5:n.127+261G>A
NM_012339.3:c.357+261G>A	NP_036471.1:n.357+261G>A
XM_005269667.3:c.97-10118G>A	XP_005269724.1:n.97-10118G>A
XM_006717738.2:c.285+261G>A	XP_006717801.1:n.285+261G>A
XR_945642.1:n.487+261G>A
NM_001351263.1:c.97-10118G>A	NP_001338192.1:n.97-10118G>A
NM_012339.4:c.357+261G>A	NP_036471.1:n.357+261G>A
NR_147091.1:n.485+261G>A
XM_017016010.1:c.357+261G>A	XP_016871499.1:n.357+261G>A
XR_001747072.1:n.488+261G>A
XR_001747073.1:n.488+261G>A
XR_001747074.1:n.485+261G>A
NM_012339.5:c.357+261G>A MANE Select	NP_036471.1:n.357+261G>A
NM_001351263.2:c.97-10118G>A	NP_001338192.1:n.97-10118G>A
NR_147091.2:n.487+261G>A