Canonical Allele Identifier: CA1984821472

Gene: TENM4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78702289C= , CM000673.2:g.78702289C=	GRCh38
NC_000011.9:g.78413334C= , CM000673.1:g.78413334C=	GRCh37
NC_000011.8:g.78090982C=	NCBI36
NG_051803.1:g.743363G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001098816.3:c.4324G= MANE Select	NP_001092286.2:p.Ala1442=
ENST00000278550.12:c.4324G= MANE Select	ENSP00000278550.7:p.Ala1442=
NM_001098816.2:c.4324G=	NP_001092286.2:p.Ala1442=
ENST00000278550.11:c.4324G=	ENSP00000278550.7:p.Ala1442=
ENST00000612046.4:c.4324G=	ENSP00000483150.1:p.Ala1442=
XM_011544924.1:c.4372G=	XP_011543226.1:p.Ala1458=
XM_011544925.1:c.4372G=	XP_011543227.1:p.Ala1458=
XM_011544927.1:c.4351G=	XP_011543229.1:p.Ala1451=
XM_011544928.1:c.4297G=	XP_011543230.1:p.Ala1433=
XM_011544929.1:c.4273G=	XP_011543231.1:p.Ala1425=
XM_011544930.1:c.4168G=	XP_011543232.1:p.Ala1390=
XM_011544931.1:c.3211G=	XP_011543233.1:p.Ala1071=
XM_011544932.1:c.1825G=	XP_011543234.1:p.Ala609=
XM_011544933.1:c.1768G=	XP_011543235.1:p.Ala590=
XM_011544933.3:c.1768G=	XP_011543235.1:p.Ala590=
XM_011544934.1:c.223G=	XP_011543236.1:p.Ala75=
XM_017017525.1:c.4399G=	XP_016873014.1:p.Ala1467=
XM_017017526.1:c.4324G=	XP_016873015.1:p.Ala1442=