Canonical Allele Identifier: CA1917819174

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485843_69485847delinsAAAGG , CM000672.2:g.69485843_69485847delinsAAAGG	GRCh38
NC_000010.10:g.71245599_71245603delinsAAAGG , CM000672.1:g.71245599_71245603delinsAAAGG	GRCh37
NC_000010.9:g.70915605_70915609delinsAAAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+628_357+632delinsAAAGG MANE Select	ENSP00000362387.2:n.357+628_357+632delinsAAAGG
ENST00000373290.6:c.357+628_357+632delinsAAAGG	ENSP00000362387.2:n.357+628_357+632delinsAAAGG
ENST00000452130.1:c.84+628_84+632delinsAAAGG	ENSP00000404528.1:n.84+628_84+632delinsAAAGG
ENST00000475069.5:n.127+628_127+632delinsAAAGG
NM_012339.3:c.357+628_357+632delinsAAAGG	NP_036471.1:n.357+628_357+632delinsAAAGG
XM_005269667.3:c.97-9751_97-9747delinsAAAGG	XP_005269724.1:n.97-9751_97-9747delinsAAAGG
XM_006717738.2:c.285+628_285+632delinsAAAGG	XP_006717801.1:n.285+628_285+632delinsAAAGG
XR_945642.1:n.487+628_487+632delinsAAAGG
NM_001351263.1:c.97-9751_97-9747delinsAAAGG	NP_001338192.1:n.97-9751_97-9747delinsAAAGG
NM_012339.4:c.357+628_357+632delinsAAAGG	NP_036471.1:n.357+628_357+632delinsAAAGG
NR_147091.1:n.485+628_485+632delinsAAAGG
XM_017016010.1:c.357+628_357+632delinsAAAGG	XP_016871499.1:n.357+628_357+632delinsAAAGG
XR_001747072.1:n.488+628_488+632delinsAAAGG
XR_001747073.1:n.488+628_488+632delinsAAAGG
XR_001747074.1:n.485+628_485+632delinsAAAGG
NM_012339.5:c.357+628_357+632delinsAAAGG MANE Select	NP_036471.1:n.357+628_357+632delinsAAAGG
NM_001351263.2:c.97-9751_97-9747delinsAAAGG	NP_001338192.1:n.97-9751_97-9747delinsAAAGG
NR_147091.2:n.487+628_487+632delinsAAAGG