Canonical Allele Identifier: CA6207006

Gene: TENM4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.78722844G>A , CM000673.2:g.78722844G>A	GRCh38
NC_000011.9:g.78433889G>A , CM000673.1:g.78433889G>A	GRCh37
NC_000011.8:g.78111537G>A	NCBI36
NG_051803.1:g.722808C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001098816.3:c.3624C>T MANE Select	NP_001092286.2:p.Gly1208=
ENST00000278550.12:c.3624C>T MANE Select	ENSP00000278550.7:p.Gly1208=
NM_001098816.2:c.3624C>T	NP_001092286.2:p.Gly1208=
ENST00000278550.11:c.3624C>T	ENSP00000278550.7:p.Gly1208=
ENST00000612046.4:c.3624C>T	ENSP00000483150.1:p.Gly1208=
XM_011544924.1:c.3672C>T	XP_011543226.1:p.Gly1224=
XM_011544925.1:c.3672C>T	XP_011543227.1:p.Gly1224=
XM_011544927.1:c.3672C>T	XP_011543229.1:p.Gly1224=
XM_011544928.1:c.3597C>T	XP_011543230.1:p.Gly1199=
XM_011544929.1:c.3573C>T	XP_011543231.1:p.Gly1191=
XM_011544930.1:c.3468C>T	XP_011543232.1:p.Gly1156=
XM_011544931.1:c.2511C>T	XP_011543233.1:p.Gly837=
XM_011544932.1:c.1125C>T	XP_011543234.1:p.Gly375=
XM_011544933.1:c.1068C>T	XP_011543235.1:p.Gly356=
XM_011544933.3:c.1068C>T	XP_011543235.1:p.Gly356=
XM_017017525.1:c.3699C>T	XP_016873014.1:p.Gly1233=
XM_017017526.1:c.3624C>T	XP_016873015.1:p.Gly1208=