Canonical Allele Identifier: CA1917807440

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69458219C= , CM000672.2:g.69458219C=	GRCh38
NC_000010.10:g.71217975C= , CM000672.1:g.71217975C=	GRCh37
NC_000010.9:g.70887981C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.96+6529C= MANE Select	ENSP00000362387.2:n.96+6529C=
ENST00000373290.6:c.96+6529C=	ENSP00000362387.2:n.96+6529C=
ENST00000478112.1:n.214+6529C=
NM_012339.3:c.96+6529C=	NP_036471.1:n.96+6529C=
XM_005269667.3:c.96+6529C=	XP_005269724.1:n.96+6529C=
XM_006717738.2:c.25-25472C=	XP_006717801.1:n.25-25472C=
XR_945642.1:n.226+6529C=
NM_001351263.1:c.96+6529C=	NP_001338192.1:n.96+6529C=
NM_012339.4:c.96+6529C=	NP_036471.1:n.96+6529C=
NR_147091.1:n.224+6529C=
XM_017016010.1:c.96+6529C=	XP_016871499.1:n.96+6529C=
XR_001747072.1:n.227+6529C=
XR_001747073.1:n.227+6529C=
XR_001747074.1:n.224+6529C=
NM_012339.5:c.96+6529C= MANE Select	NP_036471.1:n.96+6529C=
NM_001351263.2:c.96+6529C=	NP_001338192.1:n.96+6529C=
NR_147091.2:n.226+6529C=