Canonical Allele Identifier: CA1984826663

Gene: TENM4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78708470G= , CM000673.2:g.78708470G=	GRCh38
NC_000011.9:g.78419515G= , CM000673.1:g.78419515G=	GRCh37
NC_000011.8:g.78097163G=	NCBI36
NG_051803.1:g.737182C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001098816.3:c.4100C= MANE Select	NP_001092286.2:p.Thr1367=
ENST00000278550.12:c.4100C= MANE Select	ENSP00000278550.7:p.Thr1367=
NM_001098816.2:c.4100C=	NP_001092286.2:p.Thr1367=
ENST00000278550.11:c.4100C=	ENSP00000278550.7:p.Thr1367=
ENST00000612046.4:c.4100C=	ENSP00000483150.1:p.Thr1367=
XM_011544924.1:c.4148C=	XP_011543226.1:p.Thr1383=
XM_011544925.1:c.4148C=	XP_011543227.1:p.Thr1383=
XM_011544927.1:c.4127C=	XP_011543229.1:p.Thr1376=
XM_011544928.1:c.4073C=	XP_011543230.1:p.Thr1358=
XM_011544929.1:c.4049C=	XP_011543231.1:p.Thr1350=
XM_011544930.1:c.3944C=	XP_011543232.1:p.Thr1315=
XM_011544931.1:c.2987C=	XP_011543233.1:p.Thr996=
XM_011544932.1:c.1601C=	XP_011543234.1:p.Thr534=
XM_011544933.1:c.1544C=	XP_011543235.1:p.Thr515=
XM_011544933.3:c.1544C=	XP_011543235.1:p.Thr515=
XM_011544934.1:c.-2C=	XP_011543236.1:n.-2C=
XM_017017525.1:c.4175C=	XP_016873014.1:p.Thr1392=
XM_017017526.1:c.4100C=	XP_016873015.1:p.Thr1367=