Canonical Allele Identifier: CA331002040

Gene: TEX11

Linked Data

• dbSNP Id: rs888423588
• gnomAD v2: X-70073034-A-C
• gnomAD v4: X-70853184-A-C
• MyVariant Identifiers: chrX:g.70073034A>C (hg19) ; chrX:g.70853184A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853184A>C , CM000685.2:g.70853184A>C	GRCh38
NC_000023.10:g.70073034A>C , CM000685.1:g.70073034A>C	GRCh37
NC_000023.9:g.69989759A>C	NCBI36
NG_012574.1:g.60534T>G
NG_012574.2:g.60534T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374333.7:c.406-31T>G MANE Select	ENSP00000363453.2:n.406-31T>G
ENST00000344304.3:c.451-31T>G	ENSP00000340995.3:n.451-31T>G
ENST00000374333.6:c.406-31T>G	ENSP00000363453.2:n.406-31T>G
ENST00000395889.6:c.451-31T>G	ENSP00000379226.2:n.451-31T>G
NM_001003811.1:c.451-31T>G	NP_001003811.1:n.451-31T>G
NM_031276.2:c.406-31T>G	NP_112566.2:n.406-31T>G
XM_011530994.1:c.406-31T>G	XP_011529296.1:n.406-31T>G
XM_017029649.1:c.406-31T>G	XP_016885138.1:n.406-31T>G
NM_001003811.2:c.451-31T>G	NP_001003811.1:n.451-31T>G
NM_031276.3:c.406-31T>G MANE Select	NP_112566.2:n.406-31T>G