Canonical Allele Identifier: CA378903205
Gene: TEX36 HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.125661923A>G
GRCh37 chr10:g.127350492A>G
Revel Score:
ENST00000532135 0.033
ENST00000526819 0.033
ENST00000368821 (MANE Select) 0.033
ClinVar RCV:
RCV004151591
ClinVar Variation:
2307750
dbSNP:
1467354314
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125661923A>G , CM000672.2:g.125661923A>G GRCh38
NC_000010.10:g.127350492A>G , CM000672.1:g.127350492A>G GRCh37
NC_000010.9:g.127340482A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368821.4:c.106T>C MANE Select ENSP00000357811.3:p.Ser36Pro
ENST00000368821.3:c.106T>C ENSP00000357811.3:p.Ser36Pro
ENST00000526819.5:c.106T>C ENSP00000434299.1:p.Ser36Pro
ENST00000532135.5:c.106T>C ENSP00000431764.1:p.Ser36Pro
NM_001128202.1:c.106T>C NP_001121674.1:p.Ser36Pro
XM_005269816.2:c.106T>C XP_005269873.1:p.Ser36Pro
XM_005269817.3:c.106T>C XP_005269874.1:p.Ser36Pro
XM_011539800.1:c.106T>C XP_011538102.1:p.Ser36Pro
NM_001128202.2:c.106T>C NP_001121674.1:p.Ser36Pro
NM_001318133.1:c.106T>C NP_001305062.1:p.Ser36Pro
XM_005269817.4:c.106T>C XP_005269874.1:p.Ser36Pro
NM_001128202.3:c.106T>C MANE Select NP_001121674.1:p.Ser36Pro
NM_001318133.2:c.106T>C NP_001305062.1:p.Ser36Pro
Search 100 bp 5'
Search 100 bp 3'