Canonical Allele Identifier: CA8871393

Gene: SMCHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2750503C>T , CM000680.2:g.2750503C>T	GRCh38
NC_000018.9:g.2750501C>T , CM000680.1:g.2750501C>T	GRCh37
NC_000018.8:g.2740501C>T	NCBI36
NG_031972.1:g.99616C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015295.3:c.4161C>T MANE Select	NP_056110.2:p.Phe1387=
ENST00000320876.11:c.4161C>T MANE Select	ENSP00000326603.7:p.Phe1387=
NM_015295.2:c.4161C>T	NP_056110.2:p.Phe1387=
ENST00000320876.10:c.4161C>T	ENSP00000326603.6:p.Phe1387=
ENST00000577880.5:c.2574C>T	ENSP00000463049.1:p.Phe858=
ENST00000583441.2:n.1847C>T
ENST00000584897.5:c.1981C>T
ENST00000645355.1:c.74C>T
ENST00000686763.1:c.966C>T	ENSP00000510263.1:p.Phe322=
ENST00000686864.1:c.923C>T
ENST00000688342.1:c.4161C>T	ENSP00000508422.1:p.Phe1387=
ENST00000688708.1:n.2817C>T
ENST00000690757.1:n.1618C>T
ENST00000693213.1:n.3359C>T
XM_011525642.1:c.4161C>T	XP_011523944.1:p.Phe1387=
XM_011525643.1:c.4161C>T	XP_011523945.1:p.Phe1387=
XM_011525643.2:c.4161C>T	XP_011523945.1:p.Phe1387=
XM_011525644.1:c.3777C>T	XP_011523946.1:p.Phe1259=
XM_011525645.1:c.3597C>T	XP_011523947.1:p.Phe1199=
XM_011525646.1:c.4161C>T	XP_011523948.1:p.Phe1387=
XM_017025684.1:c.3597C>T	XP_016881173.1:p.Phe1199=
XR_001753172.1:n.4350C>T
XR_001753173.1:n.4350C>T
XR_001753174.1:n.4350C>T
XR_001753175.1:n.4350C>T
XR_001753176.1:n.4350C>T
XR_001753177.1:n.4350C>T
XR_001753178.1:n.4270C>T
XR_001753179.1:n.4270C>T
XR_430039.1:n.4350C>T
XR_935054.1:n.4350C>T
XR_935055.1:n.4350C>T
XR_935055.2:n.4350C>T