Canonical Allele Identifier: CA2280681243
Gene: SMCHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2697814T= , CM000680.2:g.2697814T= GRCh38
NC_000018.9:g.2697812T= , CM000680.1:g.2697812T= GRCh37
NC_000018.8:g.2687812T= NCBI36
NG_031972.1:g.46927T=

Transcript Alleles

HGVS Amino-acid change
ENST00000684915.1:n.1289-17T=
ENST00000688342.1:c.1132-17T= ENSP00000508422.1:n.1132-17T=
ENST00000693213.1:n.410-17T=
ENST00000320876.11:c.1132-17T= MANE Select ENSP00000326603.7:n.1132-17T=
ENST00000320876.10:c.1132-17T= ENSP00000326603.6:n.1132-17T=
NM_015295.2:c.1132-17T= NP_056110.2:n.1132-17T=
XM_011525642.1:c.1132-17T= XP_011523944.1:n.1132-17T=
XM_011525643.1:c.1132-17T= XP_011523945.1:n.1132-17T=
XM_011525644.1:c.748-17T= XP_011523946.1:n.748-17T=
XM_011525645.1:c.568-17T= XP_011523947.1:n.568-17T=
XM_011525646.1:c.1132-17T= XP_011523948.1:n.1132-17T=
XM_011525647.1:c.1132-17T= XP_011523949.1:n.1132-17T=
XR_430039.1:n.1321-17T=
XR_935054.1:n.1321-17T=
XR_935055.1:n.1321-17T=
XM_011525643.2:c.1132-17T= XP_011523945.1:n.1132-17T=
XM_017025684.1:c.568-17T= XP_016881173.1:n.568-17T=
XR_001753172.1:n.1321-17T=
XR_001753173.1:n.1321-17T=
XR_001753174.1:n.1321-17T=
XR_001753175.1:n.1321-17T=
XR_001753176.1:n.1321-17T=
XR_001753177.1:n.1321-17T=
XR_001753178.1:n.1321-17T=
XR_001753179.1:n.1321-17T=
XR_935055.2:n.1321-17T=
NM_015295.3:c.1132-17T= MANE Select NP_056110.2:n.1132-17T=