Canonical Allele Identifier: CA2609454737

Gene: TSPAN15

Linked Data

• gnomAD v4: 10-69485331-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69485331_69485332insG , CM000672.2:g.69485331_69485332insG	GRCh38
NC_000010.10:g.71245087_71245088insG , CM000672.1:g.71245087_71245088insG	GRCh37
NC_000010.9:g.70915093_70915094insG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000373290.7:c.357+116_357+117insG MANE Select	ENSP00000362387.2:n.357+116_357+117insG
ENST00000373290.6:c.357+116_357+117insG	ENSP00000362387.2:n.357+116_357+117insG
ENST00000452130.1:c.84+116_84+117insG	ENSP00000404528.1:n.84+116_84+117insG
ENST00000475069.5:n.127+116_127+117insG
NM_012339.3:c.357+116_357+117insG	NP_036471.1:n.357+116_357+117insG
XM_005269667.3:c.97-10263_97-10262insG	XP_005269724.1:n.97-10263_97-10262insG
XM_006717738.2:c.285+116_285+117insG	XP_006717801.1:n.285+116_285+117insG
XR_945642.1:n.487+116_487+117insG
NM_001351263.1:c.97-10263_97-10262insG	NP_001338192.1:n.97-10263_97-10262insG
NM_012339.4:c.357+116_357+117insG	NP_036471.1:n.357+116_357+117insG
NR_147091.1:n.485+116_485+117insG
XM_017016010.1:c.357+116_357+117insG	XP_016871499.1:n.357+116_357+117insG
XR_001747072.1:n.488+116_488+117insG
XR_001747073.1:n.488+116_488+117insG
XR_001747074.1:n.485+116_485+117insG
NM_012339.5:c.357+116_357+117insG MANE Select	NP_036471.1:n.357+116_357+117insG
NM_001351263.2:c.97-10263_97-10262insG	NP_001338192.1:n.97-10263_97-10262insG
NR_147091.2:n.487+116_487+117insG