Canonical Allele Identifier: CA2436261261
Gene: TEX11 HGNC NCBI

Linked Data

dbSNP Id: rs2091518283

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.70853219G>T , CM000685.2:g.70853219G>T GRCh38
NC_000023.10:g.70073069G>T , CM000685.1:g.70073069G>T GRCh37
NC_000023.9:g.69989794G>T NCBI36
NG_012574.1:g.60499C>A
NG_012574.2:g.60499C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374333.7:c.405+29C>A MANE Select ENSP00000363453.2:n.405+29C>A
ENST00000344304.3:c.450+29C>A ENSP00000340995.3:n.450+29C>A
ENST00000374333.6:c.405+29C>A ENSP00000363453.2:n.405+29C>A
ENST00000395889.6:c.450+29C>A ENSP00000379226.2:n.450+29C>A
NM_001003811.1:c.450+29C>A NP_001003811.1:n.450+29C>A
NM_031276.2:c.405+29C>A NP_112566.2:n.405+29C>A
XM_011530994.1:c.405+29C>A XP_011529296.1:n.405+29C>A
XM_017029649.1:c.405+29C>A XP_016885138.1:n.405+29C>A
NM_001003811.2:c.450+29C>A NP_001003811.1:n.450+29C>A
NM_031276.3:c.405+29C>A MANE Select NP_112566.2:n.405+29C>A