Canonical Allele Identifier: CA1917818946

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485632_69485633delinsAG , CM000672.2:g.69485632_69485633delinsAG	GRCh38
NC_000010.10:g.71245388_71245389delinsAG , CM000672.1:g.71245388_71245389delinsAG	GRCh37
NC_000010.9:g.70915394_70915395delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+417_357+418delinsAG MANE Select	ENSP00000362387.2:n.357+417_357+418delinsAG
ENST00000373290.6:c.357+417_357+418delinsAG	ENSP00000362387.2:n.357+417_357+418delinsAG
ENST00000452130.1:c.84+417_84+418delinsAG	ENSP00000404528.1:n.84+417_84+418delinsAG
ENST00000475069.5:n.127+417_127+418delinsAG
NM_012339.3:c.357+417_357+418delinsAG	NP_036471.1:n.357+417_357+418delinsAG
XM_005269667.3:c.97-9962_97-9961delinsAG	XP_005269724.1:n.97-9962_97-9961delinsAG
XM_006717738.2:c.285+417_285+418delinsAG	XP_006717801.1:n.285+417_285+418delinsAG
XR_945642.1:n.487+417_487+418delinsAG
NM_001351263.1:c.97-9962_97-9961delinsAG	NP_001338192.1:n.97-9962_97-9961delinsAG
NM_012339.4:c.357+417_357+418delinsAG	NP_036471.1:n.357+417_357+418delinsAG
NR_147091.1:n.485+417_485+418delinsAG
XM_017016010.1:c.357+417_357+418delinsAG	XP_016871499.1:n.357+417_357+418delinsAG
XR_001747072.1:n.488+417_488+418delinsAG
XR_001747073.1:n.488+417_488+418delinsAG
XR_001747074.1:n.485+417_485+418delinsAG
NM_012339.5:c.357+417_357+418delinsAG MANE Select	NP_036471.1:n.357+417_357+418delinsAG
NM_001351263.2:c.97-9962_97-9961delinsAG	NP_001338192.1:n.97-9962_97-9961delinsAG
NR_147091.2:n.487+417_487+418delinsAG