Canonical Allele Identifier: CA929626972

Gene: TSPAN15

Linked Data

• dbSNP Id: rs1841832303
• gnomAD v3: 10-69485468-C-T
• gnomAD v4: 10-69485468-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485468C>T , CM000672.2:g.69485468C>T	GRCh38
NC_000010.10:g.71245224C>T , CM000672.1:g.71245224C>T	GRCh37
NC_000010.9:g.70915230C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373290.7:c.357+253C>T MANE Select	ENSP00000362387.2:n.357+253C>T
ENST00000373290.6:c.357+253C>T	ENSP00000362387.2:n.357+253C>T
ENST00000452130.1:c.84+253C>T	ENSP00000404528.1:n.84+253C>T
ENST00000475069.5:n.127+253C>T
NM_012339.3:c.357+253C>T	NP_036471.1:n.357+253C>T
XM_005269667.3:c.97-10126C>T	XP_005269724.1:n.97-10126C>T
XM_006717738.2:c.285+253C>T	XP_006717801.1:n.285+253C>T
XR_945642.1:n.487+253C>T
NM_001351263.1:c.97-10126C>T	NP_001338192.1:n.97-10126C>T
NM_012339.4:c.357+253C>T	NP_036471.1:n.357+253C>T
NR_147091.1:n.485+253C>T
XM_017016010.1:c.357+253C>T	XP_016871499.1:n.357+253C>T
XR_001747072.1:n.488+253C>T
XR_001747073.1:n.488+253C>T
XR_001747074.1:n.485+253C>T
NM_012339.5:c.357+253C>T MANE Select	NP_036471.1:n.357+253C>T
NM_001351263.2:c.97-10126C>T	NP_001338192.1:n.97-10126C>T
NR_147091.2:n.487+253C>T