Canonical Allele Identifier: CA2576442982
Gene: SMCHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2694484del , CM000680.2:g.2694484del GRCh38
NC_000018.9:g.2694482del , CM000680.1:g.2694482del GRCh37
NC_000018.8:g.2684482del NCBI36
NG_031972.1:g.43597del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684915.1:n.1031-43del
ENST00000688342.1:c.874-43del ENSP00000508422.1:n.874-43del
ENST00000693213.1:n.152-43del
ENST00000320876.11:c.874-43del MANE Select ENSP00000326603.7:n.874-43del
ENST00000320876.10:c.874-43del ENSP00000326603.6:n.874-43del
ENST00000581226.1:n.108-43del
NM_015295.2:c.874-43del NP_056110.2:n.874-43del
XM_011525642.1:c.874-43del XP_011523944.1:n.874-43del
XM_011525643.1:c.874-43del XP_011523945.1:n.874-43del
XM_011525644.1:c.490-43del XP_011523946.1:n.490-43del
XM_011525645.1:c.310-43del XP_011523947.1:n.310-43del
XM_011525646.1:c.874-43del XP_011523948.1:n.874-43del
XM_011525647.1:c.874-43del XP_011523949.1:n.874-43del
XR_430039.1:n.1063-43del
XR_935054.1:n.1063-43del
XR_935055.1:n.1063-43del
XM_011525643.2:c.874-43del XP_011523945.1:n.874-43del
XM_017025684.1:c.310-43del XP_016881173.1:n.310-43del
XR_001753172.1:n.1063-43del
XR_001753173.1:n.1063-43del
XR_001753174.1:n.1063-43del
XR_001753175.1:n.1063-43del
XR_001753176.1:n.1063-43del
XR_001753177.1:n.1063-43del
XR_001753178.1:n.1063-43del
XR_001753179.1:n.1063-43del
XR_935055.2:n.1063-43del
NM_015295.3:c.874-43del MANE Select NP_056110.2:n.874-43del