Canonical Allele Identifier: CA1599253586

Gene: TENM2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.168073455T>G , CM000667.2:g.168073455T>G	GRCh38
NC_000005.9:g.167500460T>G , CM000667.1:g.167500460T>G	GRCh37
NC_000005.8:g.167433038T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518659.6:c.1515+11190T>G MANE Select	ENSP00000429430.1:n.1515+11190T>G
ENST00000695885.1:c.*858+11190T>G	ENSP00000512238.1:n.*858+11190T>G
ENST00000695886.1:c.1059+11190T>G	ENSP00000512239.1:n.1059+11190T>G
ENST00000695887.1:n.1254+11190T>G
ENST00000695888.1:n.1254+11190T>G
ENST00000695961.1:c.924+11190T>G	ENSP00000512289.1:n.924+11190T>G
ENST00000695962.1:c.327+11190T>G	ENSP00000512290.1:n.327+11190T>G
ENST00000403607.2:c.1014+11190T>G	ENSP00000384905.2:n.1014+11190T>G
ENST00000518659.5:c.1515+11190T>G	ENSP00000429430.1:n.1515+11190T>G
ENST00000519204.5:c.1152+11190T>G	ENSP00000428964.1:n.1152+11190T>G
ENST00000520394.5:c.819+11190T>G	ENSP00000427874.1:n.819+11190T>G
ENST00000545108.5:c.1014+11190T>G	ENSP00000438635.2:n.1014+11190T>G
NM_001080428.2:c.819+11190T>G	NP_001073897.2:n.819+11190T>G
NM_001122679.1:c.1515+11190T>G	NP_001116151.1:n.1515+11190T>G
XM_005265950.1:c.1515+11190T>G	XP_005266007.1:n.1515+11190T>G
XM_005265952.1:c.327+11190T>G	XP_005266009.1:n.327+11190T>G
XM_006714897.1:c.1515+11190T>G	XP_006714960.1:n.1515+11190T>G
XM_006714898.2:c.837+11190T>G	XP_006714961.1:n.837+11190T>G
XM_011534604.1:c.1515+11190T>G	XP_011532906.1:n.1515+11190T>G
XM_005265950.2:c.1515+11190T>G	XP_005266007.1:n.1515+11190T>G
XM_005265952.2:c.327+11190T>G	XP_005266009.1:n.327+11190T>G
XM_006714897.2:c.1515+11190T>G	XP_006714960.1:n.1515+11190T>G
XM_011534604.2:c.1515+11190T>G	XP_011532906.1:n.1515+11190T>G
XM_017009660.1:c.1515+11190T>G	XP_016865149.1:n.1515+11190T>G
XM_017009661.1:c.1515+11190T>G	XP_016865150.1:n.1515+11190T>G
XM_017009662.1:c.1305+11190T>G	XP_016865151.1:n.1305+11190T>G
XM_017009663.2:c.1290+11190T>G	XP_016865152.1:n.1290+11190T>G
XM_017009664.1:c.1152+11190T>G	XP_016865153.1:n.1152+11190T>G
XM_017009665.1:c.1059+11190T>G	XP_016865154.1:n.1059+11190T>G
XM_017009666.1:c.1059+11190T>G	XP_016865155.1:n.1059+11190T>G
XM_017009667.1:c.1059+11190T>G	XP_016865156.1:n.1059+11190T>G
XM_017009668.1:c.924+11190T>G	XP_016865157.1:n.924+11190T>G
XM_017009669.1:c.924+11190T>G	XP_016865158.1:n.924+11190T>G
NM_001080428.3:c.819+11190T>G	NP_001073897.2:n.819+11190T>G
NM_001122679.2:c.1515+11190T>G	NP_001116151.1:n.1515+11190T>G
NM_001368145.1:c.1059+11190T>G	NP_001355074.1:n.1059+11190T>G
NM_001368146.1:c.1059+11190T>G	NP_001355075.1:n.1059+11190T>G
NM_001395460.1:c.1515+11190T>G MANE Select	NP_001382389.1:n.1515+11190T>G