Canonical Allele Identifier: CA413607996

Gene: TEX11

Linked Data

• MyVariant Identifiers: chrX:g.70073000G>T (hg19) ; chrX:g.70853150G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.409C>A MANE Select	ENSP00000363453.2:p.Leu137Met
ENST00000344304.3:c.454C>A	ENSP00000340995.3:p.Leu152Met
ENST00000374333.6:c.409C>A	ENSP00000363453.2:p.Leu137Met
ENST00000395889.6:c.454C>A	ENSP00000379226.2:p.Leu152Met
NM_001003811.1:c.454C>A	NP_001003811.1:p.Leu152Met
NM_031276.2:c.409C>A	NP_112566.2:p.Leu137Met
XM_011530994.1:c.409C>A	XP_011529296.1:p.Leu137Met
XM_017029649.1:c.409C>A	XP_016885138.1:p.Leu137Met
NM_001003811.2:c.454C>A	NP_001003811.1:p.Leu152Met
NM_031276.3:c.409C>A MANE Select	NP_112566.2:p.Leu137Met