Canonical Allele Identifier: CA2280681355
Gene: SMCHD1 HGNC NCBI

Linked Data

dbSNP Id: rs2074321992

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2698105_2698106insACAACG , CM000680.2:g.2698105_2698106insACAACG GRCh38
NC_000018.9:g.2698103_2698104insACAACG , CM000680.1:g.2698103_2698104insACAACG GRCh37
NC_000018.8:g.2688103_2688104insACAACG NCBI36
NG_031972.1:g.47218_47219insACAACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000684915.1:n.1499+64_1499+65insACAACG
ENST00000688342.1:c.1342+64_1342+65insACAACG ENSP00000508422.1:n.1342+64_1342+65insACAACG
ENST00000693213.1:n.620+64_620+65insACAACG
ENST00000320876.11:c.1342+64_1342+65insACAACG MANE Select ENSP00000326603.7:n.1342+64_1342+65insACAACG
ENST00000320876.10:c.1342+64_1342+65insACAACG ENSP00000326603.6:n.1342+64_1342+65insACAACG
NM_015295.2:c.1342+64_1342+65insACAACG NP_056110.2:n.1342+64_1342+65insACAACG
XM_011525642.1:c.1342+64_1342+65insACAACG XP_011523944.1:n.1342+64_1342+65insACAACG
XM_011525643.1:c.1342+64_1342+65insACAACG XP_011523945.1:n.1342+64_1342+65insACAACG
XM_011525644.1:c.958+64_958+65insACAACG XP_011523946.1:n.958+64_958+65insACAACG
XM_011525645.1:c.778+64_778+65insACAACG XP_011523947.1:n.778+64_778+65insACAACG
XM_011525646.1:c.1342+64_1342+65insACAACG XP_011523948.1:n.1342+64_1342+65insACAACG
XM_011525647.1:c.1342+64_1342+65insACAACG XP_011523949.1:n.1342+64_1342+65insACAACG
XR_430039.1:n.1531+64_1531+65insACAACG
XR_935054.1:n.1531+64_1531+65insACAACG
XR_935055.1:n.1531+64_1531+65insACAACG
XM_011525643.2:c.1342+64_1342+65insACAACG XP_011523945.1:n.1342+64_1342+65insACAACG
XM_017025684.1:c.778+64_778+65insACAACG XP_016881173.1:n.778+64_778+65insACAACG
XR_001753172.1:n.1531+64_1531+65insACAACG
XR_001753173.1:n.1531+64_1531+65insACAACG
XR_001753174.1:n.1531+64_1531+65insACAACG
XR_001753175.1:n.1531+64_1531+65insACAACG
XR_001753176.1:n.1531+64_1531+65insACAACG
XR_001753177.1:n.1531+64_1531+65insACAACG
XR_001753178.1:n.1531+64_1531+65insACAACG
XR_001753179.1:n.1531+64_1531+65insACAACG
XR_935055.2:n.1531+64_1531+65insACAACG
NM_015295.3:c.1342+64_1342+65insACAACG MANE Select NP_056110.2:n.1342+64_1342+65insACAACG