Canonical Allele Identifier: CA1917825954

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69503554T= , CM000672.2:g.69503554T=	GRCh38
NC_000010.10:g.71263310T= , CM000672.1:g.71263310T=	GRCh37
NC_000010.9:g.70933316T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373290.7:c.571-884T= MANE Select	ENSP00000362387.2:n.571-884T=
ENST00000373290.6:c.571-884T=	ENSP00000362387.2:n.571-884T=
ENST00000452130.1:c.298-884T=	ENSP00000404528.1:n.298-884T=
ENST00000459981.1:n.503-884T=
ENST00000475069.5:n.341-884T=
ENST00000486093.5:n.280-884T=
ENST00000490083.5:n.517-884T=
NM_012339.3:c.571-884T=	NP_036471.1:n.571-884T=
XM_005269666.3:c.376-884T=	XP_005269723.1:n.376-884T=
XM_005269667.3:c.310-884T=	XP_005269724.1:n.310-884T=
XM_006717738.2:c.499-884T=	XP_006717801.1:n.499-884T=
XM_011539562.1:c.223-884T=	XP_011537864.1:n.223-884T=
XM_011539563.1:c.139-884T=	XP_011537865.1:n.139-884T=
XR_945642.1:n.772-884T=
NM_001351263.1:c.310-884T=	NP_001338192.1:n.310-884T=
NM_012339.4:c.571-884T=	NP_036471.1:n.571-884T=
NR_147091.1:n.770-884T=
XM_005269666.4:c.376-884T=	XP_005269723.1:n.376-884T=
XM_011539562.2:c.223-884T=	XP_011537864.1:n.223-884T=
XM_011539563.2:c.139-884T=	XP_011537865.1:n.139-884T=
XM_017016010.1:c.642-884T=	XP_016871499.1:n.642-884T=
XR_001747072.1:n.773-884T=
XR_001747073.1:n.773-884T=
XR_001747074.1:n.699-884T=
NM_012339.5:c.571-884T= MANE Select	NP_036471.1:n.571-884T=
NM_001351263.2:c.310-884T=	NP_001338192.1:n.310-884T=
NR_147091.2:n.772-884T=