Canonical Allele Identifier: CA642470360

Gene: TEX11

Linked Data

• dbSNP Id: rs1418774172
• gnomAD v2: X-70073027-AT-A
• gnomAD v4: X-70853177-AT-A
• MyVariant Identifiers: chrX:g.70073028del (hg19) ; chrX:g.70853178del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853178del , CM000685.2:g.70853178del	GRCh38
NC_000023.10:g.70073028del , CM000685.1:g.70073028del	GRCh37
NC_000023.9:g.69989753del	NCBI36
NG_012574.1:g.60540del
NG_012574.2:g.60540del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.406-25del MANE Select	ENSP00000363453.2:n.406-25del
ENST00000344304.3:c.451-25del	ENSP00000340995.3:n.451-25del
ENST00000374333.6:c.406-25del	ENSP00000363453.2:n.406-25del
ENST00000395889.6:c.451-25del	ENSP00000379226.2:n.451-25del
NM_001003811.1:c.451-25del	NP_001003811.1:n.451-25del
NM_031276.2:c.406-25del	NP_112566.2:n.406-25del
XM_011530994.1:c.406-25del	XP_011529296.1:n.406-25del
XM_017029649.1:c.406-25del	XP_016885138.1:n.406-25del
NM_001003811.2:c.451-25del	NP_001003811.1:n.451-25del
NM_031276.3:c.406-25del MANE Select	NP_112566.2:n.406-25del