Canonical Allele Identifier: CA382149466

Gene: TENM4

Linked Data

• MyVariant Identifiers: chr11:g.78419527A>C (hg19) ; chr11:g.78708482A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78708482A>C , CM000673.2:g.78708482A>C	GRCh38
NC_000011.9:g.78419527A>C , CM000673.1:g.78419527A>C	GRCh37
NC_000011.8:g.78097175A>C	NCBI36
NG_051803.1:g.737170T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278550.12:c.4088T>G MANE Select	ENSP00000278550.7:p.Phe1363Cys
ENST00000278550.11:c.4088T>G	ENSP00000278550.7:p.Phe1363Cys
ENST00000612046.4:c.4088T>G	ENSP00000483150.1:p.Phe1363Cys
NM_001098816.2:c.4088T>G	NP_001092286.2:p.Phe1363Cys
XM_011544924.1:c.4136T>G	XP_011543226.1:p.Phe1379Cys
XM_011544925.1:c.4136T>G	XP_011543227.1:p.Phe1379Cys
XM_011544927.1:c.4115T>G	XP_011543229.1:p.Phe1372Cys
XM_011544928.1:c.4061T>G	XP_011543230.1:p.Phe1354Cys
XM_011544929.1:c.4037T>G	XP_011543231.1:p.Phe1346Cys
XM_011544930.1:c.3932T>G	XP_011543232.1:p.Phe1311Cys
XM_011544931.1:c.2975T>G	XP_011543233.1:p.Phe992Cys
XM_011544932.1:c.1589T>G	XP_011543234.1:p.Phe530Cys
XM_011544933.1:c.1532T>G	XP_011543235.1:p.Phe511Cys
XM_011544934.1:c.-14T>G	XP_011543236.1:n.-14T>G
XM_011544933.3:c.1532T>G	XP_011543235.1:p.Phe511Cys
XM_017017525.1:c.4163T>G	XP_016873014.1:p.Phe1388Cys
XM_017017526.1:c.4088T>G	XP_016873015.1:p.Phe1363Cys
NM_001098816.3:c.4088T>G MANE Select	NP_001092286.2:p.Phe1363Cys