Canonical Allele Identifier: CA1917825925

Gene: TSPAN15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69503497G= , CM000672.2:g.69503497G=	GRCh38
NC_000010.10:g.71263253G= , CM000672.1:g.71263253G=	GRCh37
NC_000010.9:g.70933259G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.571-941G= MANE Select	ENSP00000362387.2:n.571-941G=
ENST00000373290.6:c.571-941G=	ENSP00000362387.2:n.571-941G=
ENST00000452130.1:c.298-941G=	ENSP00000404528.1:n.298-941G=
ENST00000459981.1:n.503-941G=
ENST00000475069.5:n.341-941G=
ENST00000486093.5:n.280-941G=
ENST00000490083.5:n.517-941G=
NM_012339.3:c.571-941G=	NP_036471.1:n.571-941G=
XM_005269666.3:c.376-941G=	XP_005269723.1:n.376-941G=
XM_005269667.3:c.310-941G=	XP_005269724.1:n.310-941G=
XM_006717738.2:c.499-941G=	XP_006717801.1:n.499-941G=
XM_011539562.1:c.223-941G=	XP_011537864.1:n.223-941G=
XM_011539563.1:c.139-941G=	XP_011537865.1:n.139-941G=
XR_945642.1:n.772-941G=
NM_001351263.1:c.310-941G=	NP_001338192.1:n.310-941G=
NM_012339.4:c.571-941G=	NP_036471.1:n.571-941G=
NR_147091.1:n.770-941G=
XM_005269666.4:c.376-941G=	XP_005269723.1:n.376-941G=
XM_011539562.2:c.223-941G=	XP_011537864.1:n.223-941G=
XM_011539563.2:c.139-941G=	XP_011537865.1:n.139-941G=
XM_017016010.1:c.642-941G=	XP_016871499.1:n.642-941G=
XR_001747072.1:n.773-941G=
XR_001747073.1:n.773-941G=
XR_001747074.1:n.699-941G=
NM_012339.5:c.571-941G= MANE Select	NP_036471.1:n.571-941G=
NM_001351263.2:c.310-941G=	NP_001338192.1:n.310-941G=
NR_147091.2:n.772-941G=