Canonical Allele Identifier: CA413607995

Gene: TEX11

Linked Data

• gnomAD v4: X-70853150-G-C
• MyVariant Identifiers: chrX:g.70073000G>C (hg19) ; chrX:g.70853150G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853150G>C , CM000685.2:g.70853150G>C	GRCh38
NC_000023.10:g.70073000G>C , CM000685.1:g.70073000G>C	GRCh37
NC_000023.9:g.69989725G>C	NCBI36
NG_012574.1:g.60568C>G
NG_012574.2:g.60568C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.409C>G MANE Select	ENSP00000363453.2:p.Leu137Val
ENST00000344304.3:c.454C>G	ENSP00000340995.3:p.Leu152Val
ENST00000374333.6:c.409C>G	ENSP00000363453.2:p.Leu137Val
ENST00000395889.6:c.454C>G	ENSP00000379226.2:p.Leu152Val
NM_001003811.1:c.454C>G	NP_001003811.1:p.Leu152Val
NM_031276.2:c.409C>G	NP_112566.2:p.Leu137Val
XM_011530994.1:c.409C>G	XP_011529296.1:p.Leu137Val
XM_017029649.1:c.409C>G	XP_016885138.1:p.Leu137Val
NM_001003811.2:c.454C>G	NP_001003811.1:p.Leu152Val
NM_031276.3:c.409C>G MANE Select	NP_112566.2:p.Leu137Val