Canonical Allele Identifier: CA413607884

Gene: TEX11

Linked Data

• dbSNP Id: rs1300917198
• MyVariant Identifiers: chrX:g.70072951T>C (hg19) ; chrX:g.70853101T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.70853101T>C , CM000685.2:g.70853101T>C	GRCh38
NC_000023.10:g.70072951T>C , CM000685.1:g.70072951T>C	GRCh37
NC_000023.9:g.69989676T>C	NCBI36
NG_012574.1:g.60617A>G
NG_012574.2:g.60617A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.458A>G MANE Select	ENSP00000363453.2:p.Asp153Gly
ENST00000344304.3:c.503A>G	ENSP00000340995.3:p.Asp168Gly
ENST00000374333.6:c.458A>G	ENSP00000363453.2:p.Asp153Gly
ENST00000395889.6:c.503A>G	ENSP00000379226.2:p.Asp168Gly
NM_001003811.1:c.503A>G	NP_001003811.1:p.Asp168Gly
NM_031276.2:c.458A>G	NP_112566.2:p.Asp153Gly
XM_011530994.1:c.458A>G	XP_011529296.1:p.Asp153Gly
XM_017029649.1:c.458A>G	XP_016885138.1:p.Asp153Gly
NM_001003811.2:c.503A>G	NP_001003811.1:p.Asp168Gly
NM_031276.3:c.458A>G MANE Select	NP_112566.2:p.Asp153Gly