Canonical Allele Identifier: CA2794333015

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3108960_3108961del , CM000674.2:g.3108960_3108961del	GRCh38
NC_000012.11:g.3218126_3218127del , CM000674.1:g.3218126_3218127del	GRCh37
NC_000012.10:g.3088387_3088388del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25241_-18+25242del MANE Select	ENSP00000011898.5:n.-18+25241_-18+25242del
ENST00000649909.1:c.-130+25241_-130+25242del	ENSP00000497370.1:n.-130+25241_-130+25242del
ENST00000011898.9:c.-18+25241_-18+25242del	ENSP00000011898.5:n.-18+25241_-18+25242del
ENST00000444315.6:c.-18+25241_-18+25242del	ENSP00000412908.2:n.-18+25241_-18+25242del
ENST00000537971.5:c.-18+31507_-18+31508del	ENSP00000444799.1:n.-18+31507_-18+31508del
NM_001168320.1:c.-18+31507_-18+31508del	NP_001161792.1:n.-18+31507_-18+31508del
NM_006675.4:c.-18+25241_-18+25242del	NP_006666.1:n.-18+25241_-18+25242del
XM_011520912.1:c.-349+25241_-349+25242del	XP_011519214.1:n.-349+25241_-349+25242del
XM_011520912.3:c.-349+25241_-349+25242del	XP_011519214.1:n.-349+25241_-349+25242del
NM_006675.5:c.-18+25241_-18+25242del MANE Select	NP_006666.1:n.-18+25241_-18+25242del
NM_001168320.2:c.-18+31507_-18+31508del	NP_001161792.1:n.-18+31507_-18+31508del