Canonical Allele Identifier: CA2794333036

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109282_3109283insGGTGTGTGTGTGTG , CM000674.2:g.3109282_3109283insGGTGTGTGTGTGTG	GRCh38
NC_000012.11:g.3218448_3218449insGGTGTGTGTGTGTG , CM000674.1:g.3218448_3218449insGGTGTGTGTGTGTG	GRCh37
NC_000012.10:g.3088709_3088710insGGTGTGTGTGTGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25563_-18+25564insGGTGTGTGTGTGTG MANE Select	ENSP00000011898.5:n.-18+25563_-18+25564insGGTGTGTGTGTGTG
ENST00000649909.1:c.-130+25563_-130+25564insGGTGTGTGTGTGTG	ENSP00000497370.1:n.-130+25563_-130+25564insGGTGTGTGTGTGTG
ENST00000011898.9:c.-18+25563_-18+25564insGGTGTGTGTGTGTG	ENSP00000011898.5:n.-18+25563_-18+25564insGGTGTGTGTGTGTG
ENST00000444315.6:c.-18+25563_-18+25564insGGTGTGTGTGTGTG	ENSP00000412908.2:n.-18+25563_-18+25564insGGTGTGTGTGTGTG
ENST00000537971.5:c.-18+31829_-18+31830insGGTGTGTGTGTGTG	ENSP00000444799.1:n.-18+31829_-18+31830insGGTGTGTGTGTGTG
NM_001168320.1:c.-18+31829_-18+31830insGGTGTGTGTGTGTG	NP_001161792.1:n.-18+31829_-18+31830insGGTGTGTGTGTGTG
NM_006675.4:c.-18+25563_-18+25564insGGTGTGTGTGTGTG	NP_006666.1:n.-18+25563_-18+25564insGGTGTGTGTGTGTG
XM_011520912.1:c.-349+25563_-349+25564insGGTGTGTGTGTGTG	XP_011519214.1:n.-349+25563_-349+25564insGGTGTGTGTGTGTG
XM_011520912.3:c.-349+25563_-349+25564insGGTGTGTGTGTGTG	XP_011519214.1:n.-349+25563_-349+25564insGGTGTGTGTGTGTG
NM_006675.5:c.-18+25563_-18+25564insGGTGTGTGTGTGTG MANE Select	NP_006666.1:n.-18+25563_-18+25564insGGTGTGTGTGTGTG
NM_001168320.2:c.-18+31829_-18+31830insGGTGTGTGTGTGTG	NP_001161792.1:n.-18+31829_-18+31830insGGTGTGTGTGTGTG