Canonical Allele Identifier: CA777972926

Gene: SMCHD1

Linked Data

• dbSNP Id: rs1342860322
• MyVariant Identifiers: chr18:g.2697823_2697826del (hg19) ; chr18:g.2697825_2697828del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2697825_2697828del , CM000680.2:g.2697825_2697828del	GRCh38
NC_000018.9:g.2697823_2697826del , CM000680.1:g.2697823_2697826del	GRCh37
NC_000018.8:g.2687823_2687826del	NCBI36
NG_031972.1:g.46938_46941del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684915.1:n.1289-6_1289-3del
ENST00000688342.1:c.1132-6_1132-3del	ENSP00000508422.1:n.1132-6_1132-3del
ENST00000693213.1:n.410-6_410-3del
ENST00000320876.11:c.1132-6_1132-3del MANE Select	ENSP00000326603.7:n.1132-6_1132-3del
ENST00000320876.10:c.1132-6_1132-3del	ENSP00000326603.6:n.1132-6_1132-3del
NM_015295.2:c.1132-6_1132-3del	NP_056110.2:n.1132-6_1132-3del
XM_011525642.1:c.1132-6_1132-3del	XP_011523944.1:n.1132-6_1132-3del
XM_011525643.1:c.1132-6_1132-3del	XP_011523945.1:n.1132-6_1132-3del
XM_011525644.1:c.748-6_748-3del	XP_011523946.1:n.748-6_748-3del
XM_011525645.1:c.568-6_568-3del	XP_011523947.1:n.568-6_568-3del
XM_011525646.1:c.1132-6_1132-3del	XP_011523948.1:n.1132-6_1132-3del
XM_011525647.1:c.1132-6_1132-3del	XP_011523949.1:n.1132-6_1132-3del
XR_430039.1:n.1321-6_1321-3del
XR_935054.1:n.1321-6_1321-3del
XR_935055.1:n.1321-6_1321-3del
XM_011525643.2:c.1132-6_1132-3del	XP_011523945.1:n.1132-6_1132-3del
XM_017025684.1:c.568-6_568-3del	XP_016881173.1:n.568-6_568-3del
XR_001753172.1:n.1321-6_1321-3del
XR_001753173.1:n.1321-6_1321-3del
XR_001753174.1:n.1321-6_1321-3del
XR_001753175.1:n.1321-6_1321-3del
XR_001753176.1:n.1321-6_1321-3del
XR_001753177.1:n.1321-6_1321-3del
XR_001753178.1:n.1321-6_1321-3del
XR_001753179.1:n.1321-6_1321-3del
XR_935055.2:n.1321-6_1321-3del
NM_015295.3:c.1132-6_1132-3del MANE Select	NP_056110.2:n.1132-6_1132-3del