Canonical Allele Identifier: CA401678023

Gene: SMCHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2703698C>T , CM000680.2:g.2703698C>T	GRCh38
NC_000018.9:g.2703696C>T , CM000680.1:g.2703696C>T	GRCh37
NC_000018.8:g.2693696C>T	NCBI36
NG_031972.1:g.52811C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015295.3:c.1654C>T MANE Select	NP_056110.2:p.Arg552Ter
ENST00000320876.11:c.1654C>T MANE Select	ENSP00000326603.7:p.Arg552Ter
NM_015295.2:c.1654C>T	NP_056110.2:p.Arg552Ter
ENST00000320876.10:c.1654C>T	ENSP00000326603.6:p.Arg552Ter
ENST00000577300.1:n.5C>T
ENST00000577880.5:c.67C>T	ENSP00000463049.1:p.Arg23Ter
ENST00000684915.1:n.1811C>T
ENST00000688342.1:c.1654C>T	ENSP00000508422.1:p.Arg552Ter
ENST00000693213.1:n.932C>T
XM_011525642.1:c.1654C>T	XP_011523944.1:p.Arg552Ter
XM_011525643.1:c.1654C>T	XP_011523945.1:p.Arg552Ter
XM_011525643.2:c.1654C>T	XP_011523945.1:p.Arg552Ter
XM_011525644.1:c.1270C>T	XP_011523946.1:p.Arg424Ter
XM_011525645.1:c.1090C>T	XP_011523947.1:p.Arg364Ter
XM_011525646.1:c.1654C>T	XP_011523948.1:p.Arg552Ter
XM_011525647.1:c.1654C>T	XP_011523949.1:p.Arg552Ter
XM_017025684.1:c.1090C>T	XP_016881173.1:p.Arg364Ter
XR_001753172.1:n.1843C>T
XR_001753173.1:n.1843C>T
XR_001753174.1:n.1843C>T
XR_001753175.1:n.1843C>T
XR_001753176.1:n.1843C>T
XR_001753177.1:n.1843C>T
XR_001753178.1:n.1843C>T
XR_001753179.1:n.1843C>T
XR_430039.1:n.1843C>T
XR_935054.1:n.1843C>T
XR_935055.1:n.1843C>T
XR_935055.2:n.1843C>T