Canonical Allele Identifier: CA413607885

Gene: TEX11

Linked Data

• MyVariant Identifiers: chrX:g.70072951T>G (hg19) ; chrX:g.70853101T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374333.7:c.458A>C MANE Select	ENSP00000363453.2:p.Asp153Ala
ENST00000344304.3:c.503A>C	ENSP00000340995.3:p.Asp168Ala
ENST00000374333.6:c.458A>C	ENSP00000363453.2:p.Asp153Ala
ENST00000395889.6:c.503A>C	ENSP00000379226.2:p.Asp168Ala
NM_001003811.1:c.503A>C	NP_001003811.1:p.Asp168Ala
NM_031276.2:c.458A>C	NP_112566.2:p.Asp153Ala
XM_011530994.1:c.458A>C	XP_011529296.1:p.Asp153Ala
XM_017029649.1:c.458A>C	XP_016885138.1:p.Asp153Ala
NM_001003811.2:c.503A>C	NP_001003811.1:p.Asp168Ala
NM_031276.3:c.458A>C MANE Select	NP_112566.2:p.Asp153Ala