Canonical Allele Identifier: CA251317

Gene: TENM4

Linked Data

• ClinVar Variation Id: 219133
• ClinVar RCV Id: RCV000203504
• dbSNP Id: rs763485258
• gnomAD v2: 11-78419515-G-T
• gnomAD v4: 11-78708470-G-T
• MyVariant Identifiers: chr11:g.78419515G>T (hg19) ; chr11:g.78708470G>T (hg38)
• PubMed: PMID:26188006

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78708470G>T , CM000673.2:g.78708470G>T	GRCh38
NC_000011.9:g.78419515G>T , CM000673.1:g.78419515G>T	GRCh37
NC_000011.8:g.78097163G>T	NCBI36
NG_051803.1:g.737182C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000278550.12:c.4100C>A MANE Select	ENSP00000278550.7:p.Thr1367Asn
ENST00000278550.11:c.4100C>A	ENSP00000278550.7:p.Thr1367Asn
ENST00000612046.4:c.4100C>A	ENSP00000483150.1:p.Thr1367Asn
NM_001098816.2:c.4100C>A	NP_001092286.2:p.Thr1367Asn
XM_011544924.1:c.4148C>A	XP_011543226.1:p.Thr1383Asn
XM_011544925.1:c.4148C>A	XP_011543227.1:p.Thr1383Asn
XM_011544927.1:c.4127C>A	XP_011543229.1:p.Thr1376Asn
XM_011544928.1:c.4073C>A	XP_011543230.1:p.Thr1358Asn
XM_011544929.1:c.4049C>A	XP_011543231.1:p.Thr1350Asn
XM_011544930.1:c.3944C>A	XP_011543232.1:p.Thr1315Asn
XM_011544931.1:c.2987C>A	XP_011543233.1:p.Thr996Asn
XM_011544932.1:c.1601C>A	XP_011543234.1:p.Thr534Asn
XM_011544933.1:c.1544C>A	XP_011543235.1:p.Thr515Asn
XM_011544934.1:c.-2C>A	XP_011543236.1:n.-2C>A
XM_011544933.3:c.1544C>A	XP_011543235.1:p.Thr515Asn
XM_017017525.1:c.4175C>A	XP_016873014.1:p.Thr1392Asn
XM_017017526.1:c.4100C>A	XP_016873015.1:p.Thr1367Asn
NM_001098816.3:c.4100C>A MANE Select	NP_001092286.2:p.Thr1367Asn