Canonical Allele Identifier: CA1917819111

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485777_69485779delinsGGG , CM000672.2:g.69485777_69485779delinsGGG	GRCh38
NC_000010.10:g.71245533_71245535delinsGGG , CM000672.1:g.71245533_71245535delinsGGG	GRCh37
NC_000010.9:g.70915539_70915541delinsGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+562_357+564delinsGGG MANE Select	ENSP00000362387.2:n.357+562_357+564delinsGGG
ENST00000373290.6:c.357+562_357+564delinsGGG	ENSP00000362387.2:n.357+562_357+564delinsGGG
ENST00000452130.1:c.84+562_84+564delinsGGG	ENSP00000404528.1:n.84+562_84+564delinsGGG
ENST00000475069.5:n.127+562_127+564delinsGGG
NM_012339.3:c.357+562_357+564delinsGGG	NP_036471.1:n.357+562_357+564delinsGGG
XM_005269667.3:c.97-9817_97-9815delinsGGG	XP_005269724.1:n.97-9817_97-9815delinsGGG
XM_006717738.2:c.285+562_285+564delinsGGG	XP_006717801.1:n.285+562_285+564delinsGGG
XR_945642.1:n.487+562_487+564delinsGGG
NM_001351263.1:c.97-9817_97-9815delinsGGG	NP_001338192.1:n.97-9817_97-9815delinsGGG
NM_012339.4:c.357+562_357+564delinsGGG	NP_036471.1:n.357+562_357+564delinsGGG
NR_147091.1:n.485+562_485+564delinsGGG
XM_017016010.1:c.357+562_357+564delinsGGG	XP_016871499.1:n.357+562_357+564delinsGGG
XR_001747072.1:n.488+562_488+564delinsGGG
XR_001747073.1:n.488+562_488+564delinsGGG
XR_001747074.1:n.485+562_485+564delinsGGG
NM_012339.5:c.357+562_357+564delinsGGG MANE Select	NP_036471.1:n.357+562_357+564delinsGGG
NM_001351263.2:c.97-9817_97-9815delinsGGG	NP_001338192.1:n.97-9817_97-9815delinsGGG
NR_147091.2:n.487+562_487+564delinsGGG