Canonical Allele Identifier: CA3123315985

Gene: TENM2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167783467A>C , CM000667.2:g.167783467A>C	GRCh38
NC_000005.9:g.167210472A>C , CM000667.1:g.167210472A>C	GRCh37
NC_000005.8:g.167143050A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518659.6:c.503-92519A>C MANE Select	ENSP00000429430.1:n.503-92519A>C
ENST00000695885.1:c.47-92519A>C	ENSP00000512238.1:n.47-92519A>C
ENST00000695886.1:c.47-92519A>C	ENSP00000512239.1:n.47-92519A>C
ENST00000695887.1:n.242-92519A>C
ENST00000695888.1:n.242-92519A>C
ENST00000518659.5:c.503-92519A>C	ENSP00000429430.1:n.503-92519A>C
ENST00000519204.5:c.139+28275A>C	ENSP00000428964.1:n.139+28275A>C
ENST00000520393.5:n.54-92519A>C
ENST00000520394.5:c.139+28275A>C	ENSP00000427874.1:n.139+28275A>C
NM_001080428.2:c.139+28275A>C	NP_001073897.2:n.139+28275A>C
NM_001122679.1:c.503-92519A>C	NP_001116151.1:n.503-92519A>C
XM_005265950.1:c.503-92519A>C	XP_005266007.1:n.503-92519A>C
XM_006714897.1:c.503-92519A>C	XP_006714960.1:n.503-92519A>C
XM_011534604.1:c.503-92519A>C	XP_011532906.1:n.503-92519A>C
XM_005265950.2:c.503-92519A>C	XP_005266007.1:n.503-92519A>C
XM_006714897.2:c.503-92519A>C	XP_006714960.1:n.503-92519A>C
XM_011534604.2:c.503-92519A>C	XP_011532906.1:n.503-92519A>C
XM_017009660.1:c.503-92519A>C	XP_016865149.1:n.503-92519A>C
XM_017009661.1:c.503-92519A>C	XP_016865150.1:n.503-92519A>C
XM_017009662.1:c.503-169121A>C	XP_016865151.1:n.503-169121A>C
XM_017009663.2:c.277+28411A>C	XP_016865152.1:n.277+28411A>C
XM_017009664.1:c.139+28275A>C	XP_016865153.1:n.139+28275A>C
XM_017009665.1:c.47-92519A>C	XP_016865154.1:n.47-92519A>C
XM_017009666.1:c.47-92519A>C	XP_016865155.1:n.47-92519A>C
XM_017009667.1:c.47-92519A>C	XP_016865156.1:n.47-92519A>C
XM_017009669.1:c.-90+62060A>C	XP_016865158.1:n.-90+62060A>C
NM_001080428.3:c.139+28275A>C	NP_001073897.2:n.139+28275A>C
NM_001122679.2:c.503-92519A>C	NP_001116151.1:n.503-92519A>C
NM_001368145.1:c.47-92519A>C	NP_001355074.1:n.47-92519A>C
NM_001368146.1:c.47-92519A>C	NP_001355075.1:n.47-92519A>C
NM_001395460.1:c.503-92519A>C MANE Select	NP_001382389.1:n.503-92519A>C