Canonical Allele Identifier: CA1984925511

Gene: TENM4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78948100A= , CM000673.2:g.78948100A=	GRCh38
NC_000011.9:g.78659145A= , CM000673.1:g.78659145A=	GRCh37
NC_000011.8:g.78336793A=	NCBI36
NG_051803.1:g.497552T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001098816.3:c.494-44577T= MANE Select	NP_001092286.2:n.494-44577T=
ENST00000278550.12:c.494-44577T= MANE Select	ENSP00000278550.7:n.494-44577T=
NM_001098816.2:c.494-44577T=	NP_001092286.2:n.494-44577T=
ENST00000278550.11:c.494-44577T=	ENSP00000278550.7:n.494-44577T=
ENST00000529798.1:n.400-23354T=
ENST00000533013.1:n.77+14043T=
ENST00000612046.4:c.494-44577T=	ENSP00000483150.1:n.494-44577T=
XM_011544924.1:c.569-44577T=	XP_011543226.1:n.569-44577T=
XM_011544925.1:c.569-44577T=	XP_011543227.1:n.569-44577T=
XM_011544927.1:c.569-44577T=	XP_011543229.1:n.569-44577T=
XM_011544928.1:c.494-44577T=	XP_011543230.1:n.494-44577T=
XM_011544929.1:c.569-44577T=	XP_011543231.1:n.569-44577T=
XM_011544930.1:c.364+14043T=	XP_011543232.1:n.364+14043T=
XM_017017525.1:c.569-44577T=	XP_016873014.1:n.569-44577T=
XM_017017526.1:c.494-44577T=	XP_016873015.1:n.494-44577T=