Canonical Allele Identifier: CA6327139
Gene: TECTA HGNC NCBI
TBCEL-TECTA HGNC NCBI

Linked Data

ClinVar Variation Id: 1466252
ClinVar RCV Id: RCV001963919
dbSNP Id: rs375052932
ExAC: 11:121008204 G / A
gnomAD v2: 11-121008204-G-A
gnomAD v3: 11-121137495-G-A
gnomAD v4: 11-121137495-G-A
MyVariant Identifiers: chr11:g.121008204G>A (hg19) chr11:g.121137495G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.121137495G>A , CM000673.2:g.121137495G>A GRCh38
NC_000011.9:g.121008204G>A , CM000673.1:g.121008204G>A GRCh37
NC_000011.8:g.120513414G>A NCBI36
NG_011633.1:g.39830G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392793.6:c.3016G>A (TECTA) MANE Select ENSP00000376543.1:p.Gly1006Ser
ENST00000642222.1:c.3016G>A (TECTA) ENSP00000493855.1:p.Gly1006Ser
ENST00000645008.1:c.323G>A (TECTA)
ENST00000264037.2:c.3016G>A (TECTA) ENSP00000264037.2:p.Gly1006Ser
ENST00000392793.5:c.3016G>A (TECTA) ENSP00000376543.1:p.Gly1006Ser
NM_005422.2:c.3016G>A (TECTA) NP_005413.2:p.Gly1006Ser
NM_001378761.1:c.3973G>A (TBCEL-TECTA) NP_001365690.1:p.Gly1325Ser
NM_005422.4:c.3016G>A (TECTA) MANE Select NP_005413.2:p.Gly1006Ser
Search 100 bp 5'
Search 100 bp 3'