Canonical Allele Identifier: CA1984831551

Gene: TENM4

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_001098816.3:c.3412G= MANE Select	NP_001092286.2:p.Val1138=
ENST00000278550.12:c.3412G= MANE Select	ENSP00000278550.7:p.Val1138=
NM_001098816.2:c.3412G=	NP_001092286.2:p.Val1138=
ENST00000278550.11:c.3412G=	ENSP00000278550.7:p.Val1138=
ENST00000612046.4:c.3412G=	ENSP00000483150.1:p.Val1138=
XM_011544924.1:c.3460G=	XP_011543226.1:p.Val1154=
XM_011544925.1:c.3460G=	XP_011543227.1:p.Val1154=
XM_011544927.1:c.3460G=	XP_011543229.1:p.Val1154=
XM_011544928.1:c.3385G=	XP_011543230.1:p.Val1129=
XM_011544929.1:c.3361G=	XP_011543231.1:p.Val1121=
XM_011544930.1:c.3256G=	XP_011543232.1:p.Val1086=
XM_011544931.1:c.2299G=	XP_011543233.1:p.Val767=
XM_011544932.1:c.913G=	XP_011543234.1:p.Val305=
XM_011544933.1:c.856G=	XP_011543235.1:p.Val286=
XM_011544933.3:c.856G=	XP_011543235.1:p.Val286=
XM_017017525.1:c.3487G=	XP_016873014.1:p.Val1163=
XM_017017526.1:c.3412G=	XP_016873015.1:p.Val1138=