Canonical Allele Identifier: CA2562597668

Gene: RBM6

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50038108_50038109insCCTGT , CM000665.2:g.50038108_50038109insCCTGT	GRCh38
NC_000003.11:g.50075541_50075542insCCTGT , CM000665.1:g.50075541_50075542insCCTGT	GRCh37
NC_000003.10:g.50050545_50050546insCCTGT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000266022.9:c.1558-10137_1558-10136insCCTGT MANE Select	ENSP00000266022.4:n.1558-10137_1558-10136...
ENST00000266022.8:c.1558-10137_1558-10136insCCTGT	ENSP00000266022.4:n.1558-10137_1558-10136...
ENST00000419610.5:c.45-16227_45-16226insCCTGT	ENSP00000396410.1:n.45-16227_45-16226insC...
ENST00000422955.5:c.-9-10137_-9-10136insCCTGT	ENSP00000392939.1:n.-9-10137_-9-10136insC...
ENST00000425608.5:c.1484-10137_1484-10136insCCTGT	ENSP00000408665.1:n.1484-10137_1484-10136...
ENST00000434592.5:c.-9-10137_-9-10136insCCTGT	ENSP00000399942.1:n.-9-10137_-9-10136insC...
ENST00000441115.5:n.497-10137_497-10136insCCTGT
ENST00000442092.5:c.-9-10137_-9-10136insCCTGT	ENSP00000393530.1:n.-9-10137_-9-10136insC...
ENST00000443081.5:c.1162-10137_1162-10136insCCTGT	ENSP00000396466.1:n.1162-10137_1162-10136...
ENST00000454079.5:c.1162-10137_1162-10136insCCTGT	ENSP00000406548.1:n.1162-10137_1162-10136...
ENST00000464013.5:n.183-10137_183-10136insCCTGT
ENST00000483350.1:n.63-10137_63-10136insCCTGT
NM_001167582.1:c.-9-10137_-9-10136insCCTGT	NP_001161054.1:n.-9-10137_-9-10136insCCTG...
NM_005777.2:c.1558-10137_1558-10136insCCTGT	NP_005768.1:n.1558-10137_1558-10136insCCT...
XM_005264784.1:c.1162-10137_1162-10136insCCTGT	XP_005264841.1:n.1162-10137_1162-10136ins...
XM_005264785.1:c.115-10137_115-10136insCCTGT	XP_005264842.1:n.115-10137_115-10136insCC...
XM_005264786.1:c.-9-10137_-9-10136insCCTGT	XP_005264843.1:n.-9-10137_-9-10136insCCTG...
XM_005264787.1:c.-9-10137_-9-10136insCCTGT	XP_005264844.1:n.-9-10137_-9-10136insCCTG...
XM_006712916.1:c.1162-10137_1162-10136insCCTGT	XP_006712979.1:n.1162-10137_1162-10136ins...
XR_940359.1:n.1812-10137_1812-10136insCCTGT
XR_940360.1:n.1812-10137_1812-10136insCCTGT
NM_001349190.1:c.-9-10137_-9-10136insCCTGT	NP_001336119.1:n.-9-10137_-9-10136insCCTG...
NM_001349191.1:c.-9-10137_-9-10136insCCTGT	NP_001336120.1:n.-9-10137_-9-10136insCCTG...
NM_001349192.1:c.-294-8608_-294-8607insCCTGT	NP_001336121.1:n.-294-8608_-294-8607insCC...
NM_001349193.1:c.-176-9052_-176-9051insCCTGT	NP_001336122.1:n.-176-9052_-176-9051insCC...
NM_001349194.1:c.16-10137_16-10136insCCTGT	NP_001336123.1:n.16-10137_16-10136insCCTG...
NR_146071.1:n.293-16227_293-16226insCCTGT
XM_017005496.2:c.1558-10137_1558-10136insCCTGT	XP_016860985.2:n.1558-10137_1558-10136ins...
XM_017005497.1:c.103-10137_103-10136insCCTGT	XP_016860986.1:n.103-10137_103-10136insCC...
XM_017005500.2:c.-176-9052_-176-9051insCCTGT	XP_016860989.1:n.-176-9052_-176-9051insCC...
XM_017005501.2:c.-127-8608_-127-8607insCCTGT	XP_016860990.1:n.-127-8608_-127-8607insCC...
XM_017005502.1:c.-9-10137_-9-10136insCCTGT	XP_016860991.1:n.-9-10137_-9-10136insCCTG...
XM_024453288.1:c.-294-8608_-294-8607insCCTGT	XP_024309056.1:n.-294-8608_-294-8607insCC...
XR_001739975.2:n.1703-10137_1703-10136insCCTGT
XR_002959486.1:n.1703-8608_1703-8607insCCTGT
NM_005777.3:c.1558-10137_1558-10136insCCTGT MANE Select	NP_005768.1:n.1558-10137_1558-10136insCCT...
NM_001167582.2:c.-9-10137_-9-10136insCCTGT	NP_001161054.1:n.-9-10137_-9-10136insCCTG...
NM_001349190.2:c.-9-10137_-9-10136insCCTGT	NP_001336119.1:n.-9-10137_-9-10136insCCTG...
NM_001349191.2:c.-9-10137_-9-10136insCCTGT	NP_001336120.1:n.-9-10137_-9-10136insCCTG...
NM_001349192.2:c.-294-8608_-294-8607insCCTGT	NP_001336121.1:n.-294-8608_-294-8607insCC...
NM_001349193.2:c.-176-9052_-176-9051insCCTGT	NP_001336122.1:n.-176-9052_-176-9051insCC...
NM_001349194.2:c.16-10137_16-10136insCCTGT	NP_001336123.1:n.16-10137_16-10136insCCTG...
NR_146071.2:n.187-16227_187-16226insCCTGT