Canonical Allele Identifier: CA1985130952

Gene: TENM4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.79372576T= , CM000673.2:g.79372576T=	GRCh38
NC_000011.9:g.79083620T= , CM000673.1:g.79083620T=	GRCh37
NC_000011.8:g.78761268T=	NCBI36
NG_051803.1:g.73076A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001098816.3:c.-321+67933A= MANE Select	NP_001092286.2:n.-321+67933A=
ENST00000278550.12:c.-321+67933A= MANE Select	ENSP00000278550.7:n.-321+67933A=
NM_001098816.2:c.-321+67933A=	NP_001092286.2:n.-321+67933A=
ENST00000278550.11:c.-321+67933A=	ENSP00000278550.7:n.-321+67933A=
ENST00000528688.5:n.239+66386A=
ENST00000531583.1:n.440+67933A=
XM_011544924.1:c.-149+67933A=	XP_011543226.1:n.-149+67933A=
XM_011544925.1:c.-293+67933A=	XP_011543227.1:n.-293+67933A=
XM_011544927.1:c.-149+67933A=	XP_011543229.1:n.-149+67933A=
XM_011544928.1:c.-321+67933A=	XP_011543230.1:n.-321+67933A=
XM_011544929.1:c.-149+67933A=	XP_011543231.1:n.-149+67933A=
XM_011544930.1:c.-661+67933A=	XP_011543232.1:n.-661+67933A=
XM_017017525.1:c.-149+67933A=	XP_016873014.1:n.-149+67933A=