Canonical Allele Identifier: CA1518085098

Gene: TENM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.182278998T= , CM000666.2:g.182278998T=	GRCh38
NC_000004.11:g.183200151T= , CM000666.1:g.183200151T=	GRCh37
NC_000004.10:g.183437145T=	NCBI36
NG_042859.1:g.40568T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000511685.6:c.-76+35522T= MANE Select	ENSP00000424226.1:n.-76+35522T=
ENST00000511685.5:c.-76+35522T=	ENSP00000424226.1:n.-76+35522T=
ENST00000512480.5:c.-75-44948T=	ENSP00000421320.1:n.-75-44948T=
ENST00000513201.1:n.176-44948T=
NM_001080477.3:c.-76+35522T=	NP_001073946.1:n.-76+35522T=
XM_017008385.1:c.-75-44948T=	XP_016863874.1:n.-75-44948T=
XM_017008386.1:c.-75-44948T=	XP_016863875.1:n.-75-44948T=
XM_017008387.2:c.-75-44948T=	XP_016863876.1:n.-75-44948T=
XM_017008389.1:c.-75-44948T=	XP_016863878.1:n.-75-44948T=
XM_017008390.1:c.-75-44948T=	XP_016863879.1:n.-75-44948T=
XM_017008391.1:c.-75-44948T=	XP_016863880.1:n.-75-44948T=
XM_017008392.1:c.-75-44948T=	XP_016863881.1:n.-75-44948T=
XM_017008393.1:c.-75-44948T=	XP_016863882.1:n.-75-44948T=
XM_017008394.1:c.-75-44948T=	XP_016863883.1:n.-75-44948T=
NM_001080477.4:c.-76+35522T= MANE Select	NP_001073946.1:n.-76+35522T=