Canonical Allele Identifier: CA1752584965
Gene: SMARCD3 HGNC NCBI

Linked Data

dbSNP Id: rs1803608980

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151253833_151253834insT , CM000669.2:g.151253833_151253834insT GRCh38
NC_000007.13:g.150950919_150950920insT , CM000669.1:g.150950919_150950920insT GRCh37
NC_000007.12:g.150581852_150581853insT NCBI36
NG_029468.1:g.28312_28313insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000356800.6:c.40-8163_40-8162insA ENSP00000349254.2:n.40-8163_40-8162insA
ENST00000392811.6:c.40-8163_40-8162insA ENSP00000376558.2:n.40-8163_40-8162insA
ENST00000469154.5:c.71-10133_71-10132insA ENSP00000417908.1:n.71-10133_71-10132insA
ENST00000477169.5:n.184+461_184+462insA
ENST00000491651.1:c.40-8163_40-8162insA ENSP00000419886.1:n.40-8163_40-8162insA
NM_001003802.1:c.40-8163_40-8162insA NP_001003802.1:n.40-8163_40-8162insA
NM_003078.3:c.40-8163_40-8162insA NP_003069.2:n.40-8163_40-8162insA
XM_011516521.1:c.-16-10133_-16-10132insA XP_011514823.1:n.-16-10133_-16-10132insA
XR_928174.1:n.717-480_717-479insT
XM_011516521.2:c.-16-10133_-16-10132insA XP_011514823.1:n.-16-10133_-16-10132insA
XM_024446887.1:c.40-8163_40-8162insA XP_024302655.1:n.40-8163_40-8162insA
XM_024446888.1:c.-16-10133_-16-10132insA XP_024302656.1:n.-16-10133_-16-10132insA
XM_024446889.1:c.-221-10133_-221-10132insA XP_024302657.1:n.-221-10133_-221-10132insA
NM_003078.4:c.40-8163_40-8162insA NP_003069.2:n.40-8163_40-8162insA
NM_001003802.2:c.40-8163_40-8162insA NP_001003802.1:n.40-8163_40-8162insA