Canonical Allele Identifier: CA6207166

Gene: TENM4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78732560T>C , CM000673.2:g.78732560T>C	GRCh38
NC_000011.9:g.78443605T>C , CM000673.1:g.78443605T>C	GRCh37
NC_000011.8:g.78121253T>C	NCBI36
NG_051803.1:g.713092A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001098816.3:c.2894A>G MANE Select	NP_001092286.2:p.Asn965Ser
ENST00000278550.12:c.2894A>G MANE Select	ENSP00000278550.7:p.Asn965Ser
NM_001098816.2:c.2894A>G	NP_001092286.2:p.Asn965Ser
ENST00000278550.11:c.2894A>G	ENSP00000278550.7:p.Asn965Ser
ENST00000612046.4:c.2894A>G	ENSP00000483150.1:p.Asn965Ser
XM_011544924.1:c.2942A>G	XP_011543226.1:p.Asn981Ser
XM_011544925.1:c.2942A>G	XP_011543227.1:p.Asn981Ser
XM_011544927.1:c.2942A>G	XP_011543229.1:p.Asn981Ser
XM_011544928.1:c.2867A>G	XP_011543230.1:p.Asn956Ser
XM_011544929.1:c.2843A>G	XP_011543231.1:p.Asn948Ser
XM_011544930.1:c.2738A>G	XP_011543232.1:p.Asn913Ser
XM_011544931.1:c.1781A>G	XP_011543233.1:p.Asn594Ser
XM_011544932.1:c.395A>G	XP_011543234.1:p.Asn132Ser
XM_011544933.1:c.338A>G	XP_011543235.1:p.Asn113Ser
XM_011544933.3:c.338A>G	XP_011543235.1:p.Asn113Ser
XM_017017525.1:c.2969A>G	XP_016873014.1:p.Asn990Ser
XM_017017526.1:c.2894A>G	XP_016873015.1:p.Asn965Ser