Canonical Allele Identifier: CA335302963

Gene: TENM1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.124496940G>A , CM000685.2:g.124496940G>A	GRCh38
NC_000023.10:g.123630790G>A , CM000685.1:g.123630790G>A	GRCh37
NC_000023.9:g.123458471G>A	NCBI36
NG_013249.1:g.471877C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001163278.2:c.3695+76C>T MANE Select	NP_001156750.1:n.3695+76C>T
ENST00000422452.4:c.3695+76C>T MANE Select	ENSP00000403954.4:n.3695+76C>T
NM_001163278.1:c.3695+76C>T	NP_001156750.1:n.3695+76C>T
NM_001163279.1:c.3692+76C>T	NP_001156751.1:n.3692+76C>T
NM_014253.3:c.3695+76C>T	NP_055068.2:n.3695+76C>T
ENST00000371130.7:c.3695+76C>T	ENSP00000360171.3:n.3695+76C>T
ENST00000422452.2:c.3695+76C>T	ENSP00000403954.2:n.3695+76C>T
ENST00000422452.3:c.3641+76C>T	ENSP00000403954.3:n.3641+76C>T
ENST00000461429.1:n.128+76C>T
XM_011531230.1:c.3695+76C>T	XP_011529532.1:n.3695+76C>T
XM_011531230.3:c.3695+76C>T	XP_011529532.1:n.3695+76C>T
XM_011531231.1:c.3695+76C>T	XP_011529533.1:n.3695+76C>T
XM_011531232.1:c.3695+76C>T	XP_011529534.1:n.3695+76C>T
XM_011531233.1:c.3695+76C>T	XP_011529535.1:n.3695+76C>T
XM_011531234.1:c.3695+76C>T	XP_011529536.1:n.3695+76C>T
XM_011531235.1:c.2471+76C>T	XP_011529537.1:n.2471+76C>T
XM_011531236.3:c.1301+76C>T	XP_011529538.2:n.1301+76C>T
XM_017029208.2:c.3695+76C>T	XP_016884697.1:n.3695+76C>T
XM_017029209.2:c.3695+76C>T	XP_016884698.1:n.3695+76C>T
XM_017029210.2:c.3695+76C>T	XP_016884699.1:n.3695+76C>T
XM_017029211.2:c.3695+76C>T	XP_016884700.1:n.3695+76C>T
XM_017029212.2:c.3695+76C>T	XP_016884701.1:n.3695+76C>T
XM_017029213.2:c.3695+76C>T	XP_016884702.1:n.3695+76C>T
XM_017029214.2:c.3695+76C>T	XP_016884703.1:n.3695+76C>T
XM_017029215.2:c.3695+76C>T	XP_016884704.1:n.3695+76C>T
XM_017029216.2:c.3695+76C>T	XP_016884705.1:n.3695+76C>T