Canonical Allele Identifier: CA2280666775

Gene: SMCHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2666912C= , CM000680.2:g.2666912C=	GRCh38
NC_000018.9:g.2666911C= , CM000680.1:g.2666911C=	GRCh37
NC_000018.8:g.2656911C=	NCBI36
NG_031972.1:g.16026C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684915.1:n.462C=
ENST00000688342.1:c.305C=	ENSP00000508422.1:p.Ser102=
ENST00000320876.11:c.305C= MANE Select	ENSP00000326603.7:p.Ser102=
ENST00000320876.10:c.305C=	ENSP00000326603.6:p.Ser102=
NM_015295.2:c.305C=	NP_056110.2:p.Ser102=
XM_011525642.1:c.305C=	XP_011523944.1:p.Ser102=
XM_011525643.1:c.305C=	XP_011523945.1:p.Ser102=
XM_011525644.1:c.-80C=	XP_011523946.1:n.-80C=
XM_011525646.1:c.305C=	XP_011523948.1:p.Ser102=
XM_011525647.1:c.305C=	XP_011523949.1:p.Ser102=
XR_430039.1:n.494C=
XR_935054.1:n.494C=
XR_935055.1:n.494C=
XM_011525643.2:c.305C=	XP_011523945.1:p.Ser102=
XM_017025684.1:c.-438C=	XP_016881173.1:n.-438C=
XR_001753172.1:n.494C=
XR_001753173.1:n.494C=
XR_001753174.1:n.494C=
XR_001753175.1:n.494C=
XR_001753176.1:n.494C=
XR_001753177.1:n.494C=
XR_001753178.1:n.494C=
XR_001753179.1:n.494C=
XR_935055.2:n.494C=
NM_015295.3:c.305C= MANE Select	NP_056110.2:p.Ser102=