Canonical Allele Identifier: CA3547090

Gene: TENM2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.168190459G>T , CM000667.2:g.168190459G>T	GRCh38
NC_000005.9:g.167617464G>T , CM000667.1:g.167617464G>T	GRCh37
NC_000005.8:g.167550042G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001395460.1:c.2692G>T MANE Select	NP_001382389.1:p.Ala898Ser
ENST00000518659.6:c.2692G>T MANE Select	ENSP00000429430.1:p.Ala898Ser
NM_001080428.2:c.1996G>T	NP_001073897.2:p.Ala666Ser
NM_001080428.3:c.1996G>T	NP_001073897.2:p.Ala666Ser
NM_001122679.1:c.2665G>T	NP_001116151.1:p.Ala889Ser
NM_001122679.2:c.2665G>T	NP_001116151.1:p.Ala889Ser
NM_001368145.1:c.2236G>T	NP_001355074.1:p.Ala746Ser
NM_001368146.1:c.2209G>T	NP_001355075.1:p.Ala737Ser
ENST00000403607.2:c.2164G>T	ENSP00000384905.2:p.Ala722Ser
ENST00000518659.5:c.2692G>T	ENSP00000429430.1:p.Ala898Ser
ENST00000519204.5:c.2329G>T	ENSP00000428964.1:p.Ala777Ser
ENST00000520394.5:c.1996G>T	ENSP00000427874.1:p.Ala666Ser
ENST00000521126.1:n.187G>T
ENST00000545108.5:c.2191G>T	ENSP00000438635.2:p.Ala731Ser
ENST00000695885.1:c.*2008G>T	ENSP00000512238.1:n.*2008G>T
ENST00000695886.1:c.2209G>T	ENSP00000512239.1:p.Ala737Ser
ENST00000695961.1:c.2101G>T	ENSP00000512289.1:p.Ala701Ser
ENST00000695962.1:c.1477G>T	ENSP00000512290.1:p.Ala493Ser
XM_005265950.1:c.2665G>T	XP_005266007.1:p.Ala889Ser
XM_005265950.2:c.2665G>T	XP_005266007.1:p.Ala889Ser
XM_005265952.1:c.1504G>T	XP_005266009.1:p.Ala502Ser
XM_005265952.2:c.1504G>T	XP_005266009.1:p.Ala502Ser
XM_006714897.1:c.2665G>T	XP_006714960.1:p.Ala889Ser
XM_006714897.2:c.2665G>T	XP_006714960.1:p.Ala889Ser
XM_006714898.2:c.2014G>T	XP_006714961.1:p.Ala672Ser
XM_011534604.1:c.2479G>T	XP_011532906.1:p.Ala827Ser
XM_011534604.2:c.2479G>T	XP_011532906.1:p.Ala827Ser
XM_017009660.1:c.2692G>T	XP_016865149.1:p.Ala898Ser
XM_017009661.1:c.2692G>T	XP_016865150.1:p.Ala898Ser
XM_017009662.1:c.2482G>T	XP_016865151.1:p.Ala828Ser
XM_017009663.2:c.2467G>T	XP_016865152.1:p.Ala823Ser
XM_017009664.1:c.2329G>T	XP_016865153.1:p.Ala777Ser
XM_017009665.1:c.2236G>T	XP_016865154.1:p.Ala746Ser
XM_017009666.1:c.2236G>T	XP_016865155.1:p.Ala746Ser
XM_017009667.1:c.2209G>T	XP_016865156.1:p.Ala737Ser
XM_017009668.1:c.2101G>T	XP_016865157.1:p.Ala701Ser
XM_017009669.1:c.2101G>T	XP_016865158.1:p.Ala701Ser