Canonical Allele Identifier: CA413608083
Gene: TEX11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853279A>C , CM000685.2:g.70853279A>C GRCh38
NC_000023.10:g.70073129A>C , CM000685.1:g.70073129A>C GRCh37
NC_000023.9:g.69989854A>C NCBI36
NG_012574.1:g.60439T>G
NG_012574.2:g.60439T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.374T>G MANE Select ENSP00000363453.2:p.Ile125Ser
ENST00000344304.3:c.419T>G ENSP00000340995.3:p.Ile140Ser
ENST00000374333.6:c.374T>G ENSP00000363453.2:p.Ile125Ser
ENST00000395889.6:c.419T>G ENSP00000379226.2:p.Ile140Ser
NM_001003811.1:c.419T>G NP_001003811.1:p.Ile140Ser
NM_031276.2:c.374T>G NP_112566.2:p.Ile125Ser
XM_011530994.1:c.374T>G XP_011529296.1:p.Ile125Ser
XM_017029649.1:c.374T>G XP_016885138.1:p.Ile125Ser
NM_001003811.2:c.419T>G NP_001003811.1:p.Ile140Ser
NM_031276.3:c.374T>G MANE Select NP_112566.2:p.Ile125Ser