Canonical Allele Identifier: CA1917818987

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485677_69485679delinsGAA , CM000672.2:g.69485677_69485679delinsGAA	GRCh38
NC_000010.10:g.71245433_71245435delinsGAA , CM000672.1:g.71245433_71245435delinsGAA	GRCh37
NC_000010.9:g.70915439_70915441delinsGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+462_357+464delinsGAA MANE Select	ENSP00000362387.2:n.357+462_357+464delinsGAA
ENST00000373290.6:c.357+462_357+464delinsGAA	ENSP00000362387.2:n.357+462_357+464delinsGAA
ENST00000452130.1:c.84+462_84+464delinsGAA	ENSP00000404528.1:n.84+462_84+464delinsGAA
ENST00000475069.5:n.127+462_127+464delinsGAA
NM_012339.3:c.357+462_357+464delinsGAA	NP_036471.1:n.357+462_357+464delinsGAA
XM_005269667.3:c.97-9917_97-9915delinsGAA	XP_005269724.1:n.97-9917_97-9915delinsGAA
XM_006717738.2:c.285+462_285+464delinsGAA	XP_006717801.1:n.285+462_285+464delinsGAA
XR_945642.1:n.487+462_487+464delinsGAA
NM_001351263.1:c.97-9917_97-9915delinsGAA	NP_001338192.1:n.97-9917_97-9915delinsGAA
NM_012339.4:c.357+462_357+464delinsGAA	NP_036471.1:n.357+462_357+464delinsGAA
NR_147091.1:n.485+462_485+464delinsGAA
XM_017016010.1:c.357+462_357+464delinsGAA	XP_016871499.1:n.357+462_357+464delinsGAA
XR_001747072.1:n.488+462_488+464delinsGAA
XR_001747073.1:n.488+462_488+464delinsGAA
XR_001747074.1:n.485+462_485+464delinsGAA
NM_012339.5:c.357+462_357+464delinsGAA MANE Select	NP_036471.1:n.357+462_357+464delinsGAA
NM_001351263.2:c.97-9917_97-9915delinsGAA	NP_001338192.1:n.97-9917_97-9915delinsGAA
NR_147091.2:n.487+462_487+464delinsGAA