Canonical Allele Identifier: CA2191703549

Gene: TM6SF1 HDGFL3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.83119432G= , CM000677.2:g.83119432G=	GRCh38
NC_000015.9:g.83788184G= , CM000677.1:g.83788184G=	GRCh37
NC_000015.8:g.81579188G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322019.14:c.295-146G= (TM6SF1) MANE Select	ENSP00000317000.9:n.295-146G=
ENST00000258909.13:c.295-146G= (TM6SF1)	ENSP00000258909.9:n.295-146G=
ENST00000322019.13:c.295-146G= (TM6SF1)	ENSP00000317000.9:n.295-146G=
ENST00000379384.9:c.295-146G= (TM6SF1)	ENSP00000368693.5:n.295-146G=
ENST00000379390.10:c.295-146G= (TM6SF1)	ENSP00000368700.6:n.295-146G=
ENST00000564988.5:n.407-146G= (TM6SF1)
ENST00000565774.5:c.295-146G= (TM6SF1)	ENSP00000457477.1:n.295-146G=
ENST00000565982.1:c.22-146G= (TM6SF1)	ENSP00000454275.1:n.22-146G=
ENST00000568294.5:c.394-3691C= (HDGFL3)	ENSP00000455388.1:n.394-3691C=
NM_001144903.1:c.295-146G= (TM6SF1)	NP_001138375.1:n.295-146G=
NM_023003.3:c.295-146G= (TM6SF1)	NP_075379.2:n.295-146G=
XM_006720554.2:c.607-3691C= (HDGFL3)	XP_006720617.1:n.607-3691C=
XM_011521679.1:c.295-146G= (TM6SF1)	XP_011519981.1:n.295-146G=
XM_011521680.1:c.295-146G= (TM6SF1)	XP_011519982.1:n.295-146G=
XR_429457.2:n.466-146G= (TM6SF1)
XR_931847.1:n.329-146G= (TM6SF1)
XR_931848.1:n.501-146G= (TM6SF1)
NM_001144903.2:c.295-146G= (TM6SF1)	NP_001138375.1:n.295-146G=
NM_001330385.2:c.295-146G= (TM6SF1)	NP_001317314.1:n.295-146G=
NM_001353878.1:c.295-146G= (TM6SF1)	NP_001340807.1:n.295-146G=
NM_001353879.1:c.22-146G= (TM6SF1)	NP_001340808.1:n.22-146G=
NM_001353880.1:c.22-146G= (TM6SF1)	NP_001340809.1:n.22-146G=
NM_001353881.1:c.-203-146G= (TM6SF1)	NP_001340810.1:n.-203-146G=
NM_001353882.1:c.-203-146G= (TM6SF1)	NP_001340811.1:n.-203-146G=
NM_001353883.1:c.-98-146G= (TM6SF1)	NP_001340812.1:n.-98-146G=
NM_001353884.1:c.-98-146G= (TM6SF1)	NP_001340813.1:n.-98-146G=
NM_023003.4:c.295-146G= (TM6SF1)	NP_075379.2:n.295-146G=
NR_148560.1:n.490-146G= (TM6SF1)
NR_148561.1:n.490-146G= (TM6SF1)
XM_006720554.4:c.607-3691C= (HDGFL3)	XP_006720617.1:n.607-3691C=
XM_011521679.2:c.295-146G= (TM6SF1)	XP_011519981.1:n.295-146G=
XM_017022320.1:c.295-146G= (TM6SF1)	XP_016877809.1:n.295-146G=
XM_017022321.1:c.295-146G= (TM6SF1)	XP_016877810.1:n.295-146G=
XM_017022322.1:c.295-146G= (TM6SF1)	XP_016877811.1:n.295-146G=
XM_017022325.1:c.-203-146G= (TM6SF1)	XP_016877814.1:n.-203-146G=
XM_017022329.2:c.295-146G= (TM6SF1)	XP_016877818.1:n.295-146G=
XM_017022330.1:c.295-146G= (TM6SF1)	XP_016877819.1:n.295-146G=
XM_017022331.2:c.295-146G= (TM6SF1)	XP_016877820.1:n.295-146G=
XR_001751298.2:n.772-3691C= (HDGFL3)
XR_001751318.1:n.329-146G= (TM6SF1)
XR_001751319.2:n.329-146G= (TM6SF1)
XR_001751320.1:n.389-146G= (TM6SF1)
XR_931848.2:n.389-146G= (TM6SF1)
NM_001144903.3:c.295-146G= (TM6SF1)	NP_001138375.1:n.295-146G=
NM_001330385.3:c.295-146G= (TM6SF1)	NP_001317314.1:n.295-146G=
NM_001353878.2:c.295-146G= (TM6SF1)	NP_001340807.1:n.295-146G=
NM_001353879.2:c.22-146G= (TM6SF1)	NP_001340808.1:n.22-146G=
NM_001353880.2:c.22-146G= (TM6SF1)	NP_001340809.1:n.22-146G=
NM_001353881.2:c.-203-146G= (TM6SF1)	NP_001340810.1:n.-203-146G=
NM_001353882.2:c.-203-146G= (TM6SF1)	NP_001340811.1:n.-203-146G=
NM_001353883.2:c.-98-146G= (TM6SF1)	NP_001340812.1:n.-98-146G=
NM_001353884.2:c.-98-146G= (TM6SF1)	NP_001340813.1:n.-98-146G=
NM_023003.5:c.295-146G= (TM6SF1) MANE Select	NP_075379.2:n.295-146G=
NR_148560.2:n.331-146G= (TM6SF1)
NR_148561.2:n.331-146G= (TM6SF1)