Canonical Allele Identifier: CA877776028

Gene: TEX11

Linked Data

• dbSNP Id: rs1434630787
• MyVariant Identifiers: chrX:g.70073040_70073042del (hg19) ; chrX:g.70853190_70853192del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853192_70853194del , CM000685.2:g.70853192_70853194del	GRCh38
NC_000023.10:g.70073042_70073044del , CM000685.1:g.70073042_70073044del	GRCh37
NC_000023.9:g.69989767_69989769del	NCBI36
NG_012574.1:g.60526_60528del
NG_012574.2:g.60526_60528del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.406-39_406-37del MANE Select	ENSP00000363453.2:n.406-39_406-37del
ENST00000344304.3:c.451-39_451-37del	ENSP00000340995.3:n.451-39_451-37del
ENST00000374333.6:c.406-39_406-37del	ENSP00000363453.2:n.406-39_406-37del
ENST00000395889.6:c.451-39_451-37del	ENSP00000379226.2:n.451-39_451-37del
NM_001003811.1:c.451-39_451-37del	NP_001003811.1:n.451-39_451-37del
NM_031276.2:c.406-39_406-37del	NP_112566.2:n.406-39_406-37del
XM_011530994.1:c.406-39_406-37del	XP_011529296.1:n.406-39_406-37del
XM_017029649.1:c.406-39_406-37del	XP_016885138.1:n.406-39_406-37del
NM_001003811.2:c.451-39_451-37del	NP_001003811.1:n.451-39_451-37del
NM_031276.3:c.406-39_406-37del MANE Select	NP_112566.2:n.406-39_406-37del