Canonical Allele Identifier: CA6206875

Gene: TENM4

Linked Data

• dbSNP Id: rs763485258
• ExAC: 11:78419515 G / A
• gnomAD v2: 11-78419515-G-A
• gnomAD v3: 11-78708470-G-A
• gnomAD v4: 11-78708470-G-A
• MyVariant Identifiers: chr11:g.78419515G>A (hg19) ; chr11:g.78708470G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000278550.12:c.4100C>T MANE Select	ENSP00000278550.7:p.Thr1367Ile
ENST00000278550.11:c.4100C>T	ENSP00000278550.7:p.Thr1367Ile
ENST00000612046.4:c.4100C>T	ENSP00000483150.1:p.Thr1367Ile
NM_001098816.2:c.4100C>T	NP_001092286.2:p.Thr1367Ile
XM_011544924.1:c.4148C>T	XP_011543226.1:p.Thr1383Ile
XM_011544925.1:c.4148C>T	XP_011543227.1:p.Thr1383Ile
XM_011544927.1:c.4127C>T	XP_011543229.1:p.Thr1376Ile
XM_011544928.1:c.4073C>T	XP_011543230.1:p.Thr1358Ile
XM_011544929.1:c.4049C>T	XP_011543231.1:p.Thr1350Ile
XM_011544930.1:c.3944C>T	XP_011543232.1:p.Thr1315Ile
XM_011544931.1:c.2987C>T	XP_011543233.1:p.Thr996Ile
XM_011544932.1:c.1601C>T	XP_011543234.1:p.Thr534Ile
XM_011544933.1:c.1544C>T	XP_011543235.1:p.Thr515Ile
XM_011544934.1:c.-2C>T	XP_011543236.1:n.-2C>T
XM_011544933.3:c.1544C>T	XP_011543235.1:p.Thr515Ile
XM_017017525.1:c.4175C>T	XP_016873014.1:p.Thr1392Ile
XM_017017526.1:c.4100C>T	XP_016873015.1:p.Thr1367Ile
NM_001098816.3:c.4100C>T MANE Select	NP_001092286.2:p.Thr1367Ile