Canonical Allele Identifier: CA667922441

Gene: TSPAN15

Linked Data

• dbSNP Id: rs1491169909
• MyVariant Identifiers: chr10:g.71245511_71245512insGGG (hg19) ; chr10:g.69485755_69485756insGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485757_69485759dup , CM000672.2:g.69485757_69485759dup	GRCh38
NC_000010.10:g.71245513_71245515dup , CM000672.1:g.71245513_71245515dup	GRCh37
NC_000010.9:g.70915519_70915521dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373290.7:c.357+542_357+544dup MANE Select	ENSP00000362387.2:n.357+542_357+544dup
ENST00000373290.6:c.357+542_357+544dup	ENSP00000362387.2:n.357+542_357+544dup
ENST00000452130.1:c.84+542_84+544dup	ENSP00000404528.1:n.84+542_84+544dup
ENST00000475069.5:n.127+542_127+544dup
NM_012339.3:c.357+542_357+544dup	NP_036471.1:n.357+542_357+544dup
XM_005269667.3:c.97-9837_97-9835dup	XP_005269724.1:n.97-9837_97-9835dup
XM_006717738.2:c.285+542_285+544dup	XP_006717801.1:n.285+542_285+544dup
XR_945642.1:n.487+542_487+544dup
NM_001351263.1:c.97-9837_97-9835dup	NP_001338192.1:n.97-9837_97-9835dup
NM_012339.4:c.357+542_357+544dup	NP_036471.1:n.357+542_357+544dup
NR_147091.1:n.485+542_485+544dup
XM_017016010.1:c.357+542_357+544dup	XP_016871499.1:n.357+542_357+544dup
XR_001747072.1:n.488+542_488+544dup
XR_001747073.1:n.488+542_488+544dup
XR_001747074.1:n.485+542_485+544dup
NM_012339.5:c.357+542_357+544dup MANE Select	NP_036471.1:n.357+542_357+544dup
NM_001351263.2:c.97-9837_97-9835dup	NP_001338192.1:n.97-9837_97-9835dup
NR_147091.2:n.487+542_487+544dup