Canonical Allele Identifier: CA382122587

Gene: TENM4

Linked Data

• dbSNP Id: rs538881762
• gnomAD v2: 11-78437262-C-A
• MyVariant Identifiers: chr11:g.78437262C>A (hg19) ; chr11:g.78726217C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78726217C>A , CM000673.2:g.78726217C>A	GRCh38
NC_000011.9:g.78437262C>A , CM000673.1:g.78437262C>A	GRCh37
NC_000011.8:g.78114910C>A	NCBI36
NG_051803.1:g.719435G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278550.12:c.3412G>T MANE Select	ENSP00000278550.7:p.Val1138Leu
ENST00000278550.11:c.3412G>T	ENSP00000278550.7:p.Val1138Leu
ENST00000612046.4:c.3412G>T	ENSP00000483150.1:p.Val1138Leu
NM_001098816.2:c.3412G>T	NP_001092286.2:p.Val1138Leu
XM_011544924.1:c.3460G>T	XP_011543226.1:p.Val1154Leu
XM_011544925.1:c.3460G>T	XP_011543227.1:p.Val1154Leu
XM_011544927.1:c.3460G>T	XP_011543229.1:p.Val1154Leu
XM_011544928.1:c.3385G>T	XP_011543230.1:p.Val1129Leu
XM_011544929.1:c.3361G>T	XP_011543231.1:p.Val1121Leu
XM_011544930.1:c.3256G>T	XP_011543232.1:p.Val1086Leu
XM_011544931.1:c.2299G>T	XP_011543233.1:p.Val767Leu
XM_011544932.1:c.913G>T	XP_011543234.1:p.Val305Leu
XM_011544933.1:c.856G>T	XP_011543235.1:p.Val286Leu
XM_011544933.3:c.856G>T	XP_011543235.1:p.Val286Leu
XM_017017525.1:c.3487G>T	XP_016873014.1:p.Val1163Leu
XM_017017526.1:c.3412G>T	XP_016873015.1:p.Val1138Leu
NM_001098816.3:c.3412G>T MANE Select	NP_001092286.2:p.Val1138Leu