Canonical Allele Identifier: CA502690722

Gene: SMCHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2763708G>A , CM000680.2:g.2763708G>A	GRCh38
NC_000018.9:g.2763706G>A , CM000680.1:g.2763706G>A	GRCh37
NC_000018.8:g.2753706G>A	NCBI36
NG_031972.1:g.112821G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015295.3:c.4638G>A MANE Select	NP_056110.2:p.Glu1546=
ENST00000320876.11:c.4638G>A MANE Select	ENSP00000326603.7:p.Glu1546=
NM_015295.2:c.4638G>A	NP_056110.2:p.Glu1546=
ENST00000320876.10:c.4638G>A	ENSP00000326603.6:p.Glu1546=
ENST00000577880.5:c.3051G>A	ENSP00000463049.1:p.Glu1017=
ENST00000583344.1:n.543G>A
ENST00000583344.2:n.543G>A
ENST00000584897.5:c.2458G>A
ENST00000645355.1:c.551G>A
ENST00000685656.1:n.1126G>A
ENST00000686763.1:c.*197G>A	ENSP00000510263.1:n.*197G>A
ENST00000686864.1:c.1400G>A
ENST00000688342.1:c.4506G>A	ENSP00000508422.1:p.Glu1502=
ENST00000688708.1:n.3294G>A
ENST00000688964.1:n.1338G>A
ENST00000689034.1:n.2585G>A
ENST00000693213.1:n.3836G>A
ENST00000693522.1:n.1179G>A
XM_011525642.1:c.4638G>A	XP_011523944.1:p.Glu1546=
XM_011525643.1:c.4638G>A	XP_011523945.1:p.Glu1546=
XM_011525643.2:c.4638G>A	XP_011523945.1:p.Glu1546=
XM_011525644.1:c.4254G>A	XP_011523946.1:p.Glu1418=
XM_011525645.1:c.4074G>A	XP_011523947.1:p.Glu1358=
XM_011525646.1:c.4638G>A	XP_011523948.1:p.Glu1546=
XM_017025684.1:c.4074G>A	XP_016881173.1:p.Glu1358=
XR_001753172.1:n.4827G>A
XR_001753173.1:n.4827G>A
XR_001753174.1:n.4827G>A
XR_001753175.1:n.4827G>A
XR_001753176.1:n.4827G>A
XR_001753177.1:n.4739G>A
XR_001753178.1:n.4747G>A
XR_001753179.1:n.4659G>A
XR_430039.1:n.4827G>A
XR_935054.1:n.4827G>A
XR_935055.1:n.4827G>A
XR_935055.2:n.4827G>A