Canonical Allele Identifier: CA2012557532

Gene: TSPAN9

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.3109295_3109301delinsTGTGTGA , CM000674.2:g.3109295_3109301delinsTGTGTGA	GRCh38
NC_000012.11:g.3218461_3218467delinsTGTGTGA , CM000674.1:g.3218461_3218467delinsTGTGTGA	GRCh37
NC_000012.10:g.3088722_3088728delinsTGTGTGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011898.10:c.-18+25576_-18+25582delinsTGTGTGA MANE Select	ENSP00000011898.5:n.-18+25576_-18+25582delinsTGTGTGA
ENST00000649909.1:c.-130+25576_-130+25582delinsTGTGTGA	ENSP00000497370.1:n.-130+25576_-130+25582delinsTGTGTGA
ENST00000011898.9:c.-18+25576_-18+25582delinsTGTGTGA	ENSP00000011898.5:n.-18+25576_-18+25582delinsTGTGTGA
ENST00000444315.6:c.-18+25576_-18+25582delinsTGTGTGA	ENSP00000412908.2:n.-18+25576_-18+25582delinsTGTGTGA
ENST00000537971.5:c.-18+31842_-18+31848delinsTGTGTGA	ENSP00000444799.1:n.-18+31842_-18+31848delinsTGTGTGA
NM_001168320.1:c.-18+31842_-18+31848delinsTGTGTGA	NP_001161792.1:n.-18+31842_-18+31848delinsTGTGTGA
NM_006675.4:c.-18+25576_-18+25582delinsTGTGTGA	NP_006666.1:n.-18+25576_-18+25582delinsTGTGTGA
XM_011520912.1:c.-349+25576_-349+25582delinsTGTGTGA	XP_011519214.1:n.-349+25576_-349+25582delinsTGTGTGA
XM_011520912.3:c.-349+25576_-349+25582delinsTGTGTGA	XP_011519214.1:n.-349+25576_-349+25582delinsTGTGTGA
NM_006675.5:c.-18+25576_-18+25582delinsTGTGTGA MANE Select	NP_006666.1:n.-18+25576_-18+25582delinsTGTGTGA
NM_001168320.2:c.-18+31842_-18+31848delinsTGTGTGA	NP_001161792.1:n.-18+31842_-18+31848delinsTGTGTGA