Canonical Allele Identifier: CA413608022

Gene: TEX11

Linked Data

• MyVariant Identifiers: chrX:g.70073100C>G (hg19) ; chrX:g.70853250C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853250C>G , CM000685.2:g.70853250C>G	GRCh38
NC_000023.10:g.70073100C>G , CM000685.1:g.70073100C>G	GRCh37
NC_000023.9:g.69989825C>G	NCBI36
NG_012574.1:g.60468G>C
NG_012574.2:g.60468G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374333.7:c.403G>C MANE Select	ENSP00000363453.2:p.Ala135Pro
ENST00000344304.3:c.448G>C	ENSP00000340995.3:p.Ala150Pro
ENST00000374333.6:c.403G>C	ENSP00000363453.2:p.Ala135Pro
ENST00000395889.6:c.448G>C	ENSP00000379226.2:p.Ala150Pro
NM_001003811.1:c.448G>C	NP_001003811.1:p.Ala150Pro
NM_031276.2:c.403G>C	NP_112566.2:p.Ala135Pro
XM_011530994.1:c.403G>C	XP_011529296.1:p.Ala135Pro
XM_017029649.1:c.403G>C	XP_016885138.1:p.Ala135Pro
NM_001003811.2:c.448G>C	NP_001003811.1:p.Ala150Pro
NM_031276.3:c.403G>C MANE Select	NP_112566.2:p.Ala135Pro