Canonical Allele Identifier: CA2609454734

Gene: TSPAN15

Linked Data

• gnomAD v4: 10-69485330-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485330A>G , CM000672.2:g.69485330A>G	GRCh38
NC_000010.10:g.71245086A>G , CM000672.1:g.71245086A>G	GRCh37
NC_000010.9:g.70915092A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373290.7:c.357+115A>G MANE Select	ENSP00000362387.2:n.357+115A>G
ENST00000373290.6:c.357+115A>G	ENSP00000362387.2:n.357+115A>G
ENST00000452130.1:c.84+115A>G	ENSP00000404528.1:n.84+115A>G
ENST00000475069.5:n.127+115A>G
NM_012339.3:c.357+115A>G	NP_036471.1:n.357+115A>G
XM_005269667.3:c.97-10264A>G	XP_005269724.1:n.97-10264A>G
XM_006717738.2:c.285+115A>G	XP_006717801.1:n.285+115A>G
XR_945642.1:n.487+115A>G
NM_001351263.1:c.97-10264A>G	NP_001338192.1:n.97-10264A>G
NM_012339.4:c.357+115A>G	NP_036471.1:n.357+115A>G
NR_147091.1:n.485+115A>G
XM_017016010.1:c.357+115A>G	XP_016871499.1:n.357+115A>G
XR_001747072.1:n.488+115A>G
XR_001747073.1:n.488+115A>G
XR_001747074.1:n.485+115A>G
NM_012339.5:c.357+115A>G MANE Select	NP_036471.1:n.357+115A>G
NM_001351263.2:c.97-10264A>G	NP_001338192.1:n.97-10264A>G
NR_147091.2:n.487+115A>G