Canonical Allele Identifier: CA1598904507

Gene: TENM2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167317736T= , CM000667.2:g.167317736T=	GRCh38
NC_000005.9:g.166744741T= , CM000667.1:g.166744741T=	GRCh37
NC_000005.8:g.166677319T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518659.6:c.226+32673T= MANE Select	ENSP00000429430.1:n.226+32673T=
ENST00000695884.1:n.878+32673T=
ENST00000518659.5:c.226+32673T=	ENSP00000429430.1:n.226+32673T=
NM_001122679.1:c.226+32673T=	NP_001116151.1:n.226+32673T=
XM_005265950.1:c.226+32673T=	XP_005266007.1:n.226+32673T=
XM_006714897.1:c.226+32673T=	XP_006714960.1:n.226+32673T=
XM_011534604.1:c.226+32673T=	XP_011532906.1:n.226+32673T=
XM_005265950.2:c.226+32673T=	XP_005266007.1:n.226+32673T=
XM_006714897.2:c.226+32673T=	XP_006714960.1:n.226+32673T=
XM_011534604.2:c.226+32673T=	XP_011532906.1:n.226+32673T=
XM_017009660.1:c.226+32673T=	XP_016865149.1:n.226+32673T=
XM_017009661.1:c.226+32673T=	XP_016865150.1:n.226+32673T=
XM_017009662.1:c.226+32673T=	XP_016865151.1:n.226+32673T=
NM_001122679.2:c.226+32673T=	NP_001116151.1:n.226+32673T=
NM_001395460.1:c.226+32673T= MANE Select	NP_001382389.1:n.226+32673T=