Canonical Allele Identifier: CA131783127

Gene: TENM2

Linked Data

• dbSNP Id: rs1549309
• gnomAD v2: 5-167226979-G-A
• gnomAD v3: 5-167799974-G-A
• gnomAD v4: 5-167799974-G-A
• MyVariant Identifiers: chr5:g.167226979G>A (hg19) ; chr5:g.167799974G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.167799974G>A , CM000667.2:g.167799974G>A	GRCh38
NC_000005.9:g.167226979G>A , CM000667.1:g.167226979G>A	GRCh37
NC_000005.8:g.167159557G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000518659.6:c.503-76012G>A MANE Select	ENSP00000429430.1:n.503-76012G>A
ENST00000695885.1:c.47-76012G>A	ENSP00000512238.1:n.47-76012G>A
ENST00000695886.1:c.47-76012G>A	ENSP00000512239.1:n.47-76012G>A
ENST00000695887.1:n.242-76012G>A
ENST00000695888.1:n.242-76012G>A
ENST00000518659.5:c.503-76012G>A	ENSP00000429430.1:n.503-76012G>A
ENST00000519204.5:c.139+44782G>A	ENSP00000428964.1:n.139+44782G>A
ENST00000520393.5:n.54-76012G>A
ENST00000520394.5:c.139+44782G>A	ENSP00000427874.1:n.139+44782G>A
NM_001080428.2:c.139+44782G>A	NP_001073897.2:n.139+44782G>A
NM_001122679.1:c.503-76012G>A	NP_001116151.1:n.503-76012G>A
XM_005265950.1:c.503-76012G>A	XP_005266007.1:n.503-76012G>A
XM_006714897.1:c.503-76012G>A	XP_006714960.1:n.503-76012G>A
XM_011534604.1:c.503-76012G>A	XP_011532906.1:n.503-76012G>A
XM_005265950.2:c.503-76012G>A	XP_005266007.1:n.503-76012G>A
XM_006714897.2:c.503-76012G>A	XP_006714960.1:n.503-76012G>A
XM_011534604.2:c.503-76012G>A	XP_011532906.1:n.503-76012G>A
XM_017009660.1:c.503-76012G>A	XP_016865149.1:n.503-76012G>A
XM_017009661.1:c.503-76012G>A	XP_016865150.1:n.503-76012G>A
XM_017009662.1:c.503-152614G>A	XP_016865151.1:n.503-152614G>A
XM_017009663.2:c.277+44918G>A	XP_016865152.1:n.277+44918G>A
XM_017009664.1:c.139+44782G>A	XP_016865153.1:n.139+44782G>A
XM_017009665.1:c.47-76012G>A	XP_016865154.1:n.47-76012G>A
XM_017009666.1:c.47-76012G>A	XP_016865155.1:n.47-76012G>A
XM_017009667.1:c.47-76012G>A	XP_016865156.1:n.47-76012G>A
XM_017009669.1:c.-89-76012G>A	XP_016865158.1:n.-89-76012G>A
NM_001080428.3:c.139+44782G>A	NP_001073897.2:n.139+44782G>A
NM_001122679.2:c.503-76012G>A	NP_001116151.1:n.503-76012G>A
NM_001368145.1:c.47-76012G>A	NP_001355074.1:n.47-76012G>A
NM_001368146.1:c.47-76012G>A	NP_001355075.1:n.47-76012G>A
NM_001395460.1:c.503-76012G>A MANE Select	NP_001382389.1:n.503-76012G>A