Canonical Allele Identifier: CA2280666805

Gene: SMCHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2667022A= , CM000680.2:g.2667022A=	GRCh38
NC_000018.9:g.2667021A= , CM000680.1:g.2667021A=	GRCh37
NC_000018.8:g.2657021A=	NCBI36
NG_031972.1:g.16136A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000684915.1:n.572A=
ENST00000688342.1:c.415A=	ENSP00000508422.1:p.Asn139=
ENST00000320876.11:c.415A= MANE Select	ENSP00000326603.7:p.Asn139=
ENST00000320876.10:c.415A=	ENSP00000326603.6:p.Asn139=
NM_015295.2:c.415A=	NP_056110.2:p.Asn139=
XM_011525642.1:c.415A=	XP_011523944.1:p.Asn139=
XM_011525643.1:c.415A=	XP_011523945.1:p.Asn139=
XM_011525644.1:c.31A=	XP_011523946.1:p.Asn11=
XM_011525645.1:c.-328A=	XP_011523947.1:n.-328A=
XM_011525646.1:c.415A=	XP_011523948.1:p.Asn139=
XM_011525647.1:c.415A=	XP_011523949.1:p.Asn139=
XR_430039.1:n.604A=
XR_935054.1:n.604A=
XR_935055.1:n.604A=
XM_011525643.2:c.415A=	XP_011523945.1:p.Asn139=
XM_017025684.1:c.-328A=	XP_016881173.1:n.-328A=
XR_001753172.1:n.604A=
XR_001753173.1:n.604A=
XR_001753174.1:n.604A=
XR_001753175.1:n.604A=
XR_001753176.1:n.604A=
XR_001753177.1:n.604A=
XR_001753178.1:n.604A=
XR_001753179.1:n.604A=
XR_935055.2:n.604A=
NM_015295.3:c.415A= MANE Select	NP_056110.2:p.Asn139=