Canonical Allele Identifier: CA401694618
Gene: SMCHD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2694590G>A , CM000680.2:g.2694590G>A GRCh38
NC_000018.9:g.2694588G>A , CM000680.1:g.2694588G>A GRCh37
NC_000018.8:g.2684588G>A NCBI36
NG_031972.1:g.43703G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684915.1:n.1094G>A
ENST00000688342.1:c.937G>A ENSP00000508422.1:p.Glu313Lys
ENST00000693213.1:n.215G>A
ENST00000320876.11:c.937G>A MANE Select ENSP00000326603.7:p.Glu313Lys
ENST00000320876.10:c.937G>A ENSP00000326603.6:p.Glu313Lys
ENST00000581226.1:n.171G>A
NM_015295.2:c.937G>A NP_056110.2:p.Glu313Lys
XM_011525642.1:c.937G>A XP_011523944.1:p.Glu313Lys
XM_011525643.1:c.937G>A XP_011523945.1:p.Glu313Lys
XM_011525644.1:c.553G>A XP_011523946.1:p.Glu185Lys
XM_011525645.1:c.373G>A XP_011523947.1:p.Glu125Lys
XM_011525646.1:c.937G>A XP_011523948.1:p.Glu313Lys
XM_011525647.1:c.937G>A XP_011523949.1:p.Glu313Lys
XR_430039.1:n.1126G>A
XR_935054.1:n.1126G>A
XR_935055.1:n.1126G>A
XM_011525643.2:c.937G>A XP_011523945.1:p.Glu313Lys
XM_017025684.1:c.373G>A XP_016881173.1:p.Glu125Lys
XR_001753172.1:n.1126G>A
XR_001753173.1:n.1126G>A
XR_001753174.1:n.1126G>A
XR_001753175.1:n.1126G>A
XR_001753176.1:n.1126G>A
XR_001753177.1:n.1126G>A
XR_001753178.1:n.1126G>A
XR_001753179.1:n.1126G>A
XR_935055.2:n.1126G>A
NM_015295.3:c.937G>A MANE Select NP_056110.2:p.Glu313Lys