Canonical Allele Identifier: CA2503250096
Gene: SMCHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2698149_2698150insTAGCTATAG , CM000680.2:g.2698149_2698150insTAGCTATAG GRCh38
NC_000018.9:g.2698147_2698148insTAGCTATAG , CM000680.1:g.2698147_2698148insTAGCTATAG GRCh37
NC_000018.8:g.2688147_2688148insTAGCTATAG NCBI36
NG_031972.1:g.47262_47263insTAGCTATAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000684915.1:n.1499+108_1499+109insTAGCTATAG
ENST00000688342.1:c.1342+108_1342+109insTAGCTATAG ENSP00000508422.1:n.1342+108_1342+109insTAGCTATAG
ENST00000693213.1:n.620+108_620+109insTAGCTATAG
ENST00000320876.11:c.1342+108_1342+109insTAGCTATAG MANE Select ENSP00000326603.7:n.1342+108_1342+109insTAGCTATAG
ENST00000320876.10:c.1342+108_1342+109insTAGCTATAG ENSP00000326603.6:n.1342+108_1342+109insTAGCTATAG
NM_015295.2:c.1342+108_1342+109insTAGCTATAG NP_056110.2:n.1342+108_1342+109insTAGCTATAG
XM_011525642.1:c.1342+108_1342+109insTAGCTATAG XP_011523944.1:n.1342+108_1342+109insTAGCTATAG
XM_011525643.1:c.1342+108_1342+109insTAGCTATAG XP_011523945.1:n.1342+108_1342+109insTAGCTATAG
XM_011525644.1:c.958+108_958+109insTAGCTATAG XP_011523946.1:n.958+108_958+109insTAGCTATAG
XM_011525645.1:c.778+108_778+109insTAGCTATAG XP_011523947.1:n.778+108_778+109insTAGCTATAG
XM_011525646.1:c.1342+108_1342+109insTAGCTATAG XP_011523948.1:n.1342+108_1342+109insTAGCTATAG
XM_011525647.1:c.1342+108_1342+109insTAGCTATAG XP_011523949.1:n.1342+108_1342+109insTAGCTATAG
XR_430039.1:n.1531+108_1531+109insTAGCTATAG
XR_935054.1:n.1531+108_1531+109insTAGCTATAG
XR_935055.1:n.1531+108_1531+109insTAGCTATAG
XM_011525643.2:c.1342+108_1342+109insTAGCTATAG XP_011523945.1:n.1342+108_1342+109insTAGCTATAG
XM_017025684.1:c.778+108_778+109insTAGCTATAG XP_016881173.1:n.778+108_778+109insTAGCTATAG
XR_001753172.1:n.1531+108_1531+109insTAGCTATAG
XR_001753173.1:n.1531+108_1531+109insTAGCTATAG
XR_001753174.1:n.1531+108_1531+109insTAGCTATAG
XR_001753175.1:n.1531+108_1531+109insTAGCTATAG
XR_001753176.1:n.1531+108_1531+109insTAGCTATAG
XR_001753177.1:n.1531+108_1531+109insTAGCTATAG
XR_001753178.1:n.1531+108_1531+109insTAGCTATAG
XR_001753179.1:n.1531+108_1531+109insTAGCTATAG
XR_935055.2:n.1531+108_1531+109insTAGCTATAG
NM_015295.3:c.1342+108_1342+109insTAGCTATAG MANE Select NP_056110.2:n.1342+108_1342+109insTAGCTATAG