Canonical Allele Identifier: CA360420099

Gene: TMEM161B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.88207164A>C , CM000667.2:g.88207164A>C	GRCh38
NC_000005.9:g.87502981A>C , CM000667.1:g.87502981A>C	GRCh37
NC_000005.8:g.87538737A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_153354.5:c.463T>G MANE Select	NP_699185.1:p.Leu155Val
ENST00000296595.11:c.463T>G MANE Select	ENSP00000296595.6:p.Leu155Val
NM_001289007.1:c.463T>G	NP_001275936.1:p.Leu155Val
NM_001289007.2:c.463T>G	NP_001275936.1:p.Leu155Val
NM_001289008.1:c.430T>G	NP_001275937.1:p.Leu144Val
NM_001289008.2:c.430T>G	NP_001275937.1:p.Leu144Val
NM_001349400.1:c.-62-22T>G	NP_001336329.1:n.-62-22T>G
NM_001349400.2:c.-62-22T>G	NP_001336329.1:n.-62-22T>G
NM_001349402.1:c.-62-22T>G	NP_001336331.1:n.-62-22T>G
NM_001349402.2:c.-62-22T>G	NP_001336331.1:n.-62-22T>G
NM_001349403.1:c.-62-22T>G	NP_001336332.1:n.-62-22T>G
NM_001349403.2:c.-62-22T>G	NP_001336332.1:n.-62-22T>G
NM_001349405.1:c.-62-22T>G	NP_001336334.1:n.-62-22T>G
NM_001349405.2:c.-62-22T>G	NP_001336334.1:n.-62-22T>G
NM_001349407.1:c.463T>G	NP_001336336.1:p.Leu155Val
NM_001349407.2:c.463T>G	NP_001336336.1:p.Leu155Val
NM_153354.4:c.463T>G	NP_699185.1:p.Leu155Val
NR_110266.1:n.706T>G
NR_110266.2:n.672T>G
ENST00000296595.10:c.463T>G	ENSP00000296595.6:p.Leu155Val
ENST00000503755.5:n.367T>G
ENST00000506536.5:c.-62-22T>G	ENSP00000421733.1:n.-62-22T>G
ENST00000507872.1:c.447-22T>G	ENSP00000427312.1:n.447-22T>G
ENST00000509387.5:c.82T>G	ENSP00000424200.1:p.Leu28Val
ENST00000510089.5:c.82T>G	ENSP00000423380.1:p.Leu28Val
ENST00000511087.5:c.*184T>G	ENSP00000421805.1:n.*184T>G
ENST00000511218.5:c.-62-22T>G	ENSP00000425991.1:n.-62-22T>G
ENST00000512429.5:c.430T>G	ENSP00000421498.1:p.Leu144Val
ENST00000513487.5:n.417T>G
ENST00000514135.5:c.463T>G	ENSP00000426354.1:p.Leu155Val
XM_006714553.1:c.463T>G	XP_006714616.1:p.Leu155Val
XM_006714554.2:c.82T>G	XP_006714617.1:p.Leu28Val
XM_006714555.2:c.82T>G	XP_006714618.1:p.Leu28Val
XM_006714556.2:c.82T>G	XP_006714619.1:p.Leu28Val
XM_011543201.1:c.82T>G	XP_011541503.1:p.Leu28Val
XM_011543202.1:c.82T>G	XP_011541504.1:p.Leu28Val
XM_011543203.1:c.28T>G	XP_011541505.1:p.Leu10Val
XM_011543204.1:c.-62-22T>G	XP_011541506.1:n.-62-22T>G
XM_011543204.3:c.-62-22T>G	XP_011541506.2:n.-62-22T>G
XM_011543205.1:c.463T>G	XP_011541507.1:p.Leu155Val
XM_011543206.1:c.463T>G	XP_011541508.1:p.Leu155Val
XM_017009093.2:c.463T>G	XP_016864582.1:p.Leu155Val
XM_017009094.2:c.544T>G	XP_016864583.2:p.Leu182Val
XM_017009097.2:c.82T>G	XP_016864586.1:p.Leu28Val
XM_017009100.2:c.544T>G	XP_016864589.2:p.Leu182Val
XM_017009102.2:c.-62-22T>G	XP_016864591.1:n.-62-22T>G
XM_017009104.2:c.-435T>G	XP_016864593.1:n.-435T>G
XM_024454371.1:c.544T>G	XP_024310139.1:p.Leu182Val
XM_024454372.1:c.430T>G	XP_024310140.1:p.Leu144Val
XM_024454373.1:c.544T>G	XP_024310141.1:p.Leu182Val
XM_024454374.1:c.430T>G	XP_024310142.1:p.Leu144Val
XM_024454375.1:c.430T>G	XP_024310143.1:p.Leu144Val
XM_024454376.1:c.544T>G	XP_024310144.1:p.Leu182Val
XM_024454377.1:c.-62-22T>G	XP_024310145.1:n.-62-22T>G
XM_024454378.1:c.430T>G	XP_024310146.1:p.Leu144Val
XR_001742013.2:n.569T>G
XR_001742014.2:n.569T>G
XR_002959844.1:n.1170T>G