Canonical Allele Identifier: CA1917819171

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485841A= , CM000672.2:g.69485841A=	GRCh38
NC_000010.10:g.71245597A= , CM000672.1:g.71245597A=	GRCh37
NC_000010.9:g.70915603A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+626A= MANE Select	ENSP00000362387.2:n.357+626A=
ENST00000373290.6:c.357+626A=	ENSP00000362387.2:n.357+626A=
ENST00000452130.1:c.84+626A=	ENSP00000404528.1:n.84+626A=
ENST00000475069.5:n.127+626A=
NM_012339.3:c.357+626A=	NP_036471.1:n.357+626A=
XM_005269667.3:c.97-9753A=	XP_005269724.1:n.97-9753A=
XM_006717738.2:c.285+626A=	XP_006717801.1:n.285+626A=
XR_945642.1:n.487+626A=
NM_001351263.1:c.97-9753A=	NP_001338192.1:n.97-9753A=
NM_012339.4:c.357+626A=	NP_036471.1:n.357+626A=
NR_147091.1:n.485+626A=
XM_017016010.1:c.357+626A=	XP_016871499.1:n.357+626A=
XR_001747072.1:n.488+626A=
XR_001747073.1:n.488+626A=
XR_001747074.1:n.485+626A=
NM_012339.5:c.357+626A= MANE Select	NP_036471.1:n.357+626A=
NM_001351263.2:c.97-9753A=	NP_001338192.1:n.97-9753A=
NR_147091.2:n.487+626A=