Canonical Allele Identifier: CA642470361

Gene: TEX11

Linked Data

• dbSNP Id: rs1463348289
• gnomAD v2: X-70073033-C-A
• gnomAD v4: X-70853183-C-A
• MyVariant Identifiers: chrX:g.70073033C>A (hg19) ; chrX:g.70853183C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853183C>A , CM000685.2:g.70853183C>A	GRCh38
NC_000023.10:g.70073033C>A , CM000685.1:g.70073033C>A	GRCh37
NC_000023.9:g.69989758C>A	NCBI36
NG_012574.1:g.60535G>T
NG_012574.2:g.60535G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374333.7:c.406-30G>T MANE Select	ENSP00000363453.2:n.406-30G>T
ENST00000344304.3:c.451-30G>T	ENSP00000340995.3:n.451-30G>T
ENST00000374333.6:c.406-30G>T	ENSP00000363453.2:n.406-30G>T
ENST00000395889.6:c.451-30G>T	ENSP00000379226.2:n.451-30G>T
NM_001003811.1:c.451-30G>T	NP_001003811.1:n.451-30G>T
NM_031276.2:c.406-30G>T	NP_112566.2:n.406-30G>T
XM_011530994.1:c.406-30G>T	XP_011529296.1:n.406-30G>T
XM_017029649.1:c.406-30G>T	XP_016885138.1:n.406-30G>T
NM_001003811.2:c.451-30G>T	NP_001003811.1:n.451-30G>T
NM_031276.3:c.406-30G>T MANE Select	NP_112566.2:n.406-30G>T