Canonical Allele Identifier: CA642470362

Gene: TEX11

Linked Data

• dbSNP Id: rs1388341157
• gnomAD v2: X-70073039-G-A
• gnomAD v4: X-70853189-G-A
• MyVariant Identifiers: chrX:g.70073039G>A (hg19) ; chrX:g.70853189G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853189G>A , CM000685.2:g.70853189G>A	GRCh38
NC_000023.10:g.70073039G>A , CM000685.1:g.70073039G>A	GRCh37
NC_000023.9:g.69989764G>A	NCBI36
NG_012574.1:g.60529C>T
NG_012574.2:g.60529C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.406-36C>T MANE Select	ENSP00000363453.2:n.406-36C>T
ENST00000344304.3:c.451-36C>T	ENSP00000340995.3:n.451-36C>T
ENST00000374333.6:c.406-36C>T	ENSP00000363453.2:n.406-36C>T
ENST00000395889.6:c.451-36C>T	ENSP00000379226.2:n.451-36C>T
NM_001003811.1:c.451-36C>T	NP_001003811.1:n.451-36C>T
NM_031276.2:c.406-36C>T	NP_112566.2:n.406-36C>T
XM_011530994.1:c.406-36C>T	XP_011529296.1:n.406-36C>T
XM_017029649.1:c.406-36C>T	XP_016885138.1:n.406-36C>T
NM_001003811.2:c.451-36C>T	NP_001003811.1:n.451-36C>T
NM_031276.3:c.406-36C>T MANE Select	NP_112566.2:n.406-36C>T