Canonical Allele Identifier: CA2270105538
Gene: SMARCD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63837447C= , CM000679.2:g.63837447C= GRCh38
NC_000017.10:g.61914807C= , CM000679.1:g.61914807C= GRCh37
NC_000017.9:g.59268539C= NCBI36
NG_053004.1:g.10545G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697953.1:n.283G=
ENST00000698015.1:n.29G=
ENST00000698016.1:c.254G= ENSP00000513502.1:p.Arg85=
ENST00000698021.1:c.58G=
ENST00000698022.1:c.212G= ENSP00000513504.1:p.Arg71=
ENST00000698027.1:c.254G= ENSP00000513505.1:p.Arg85=
ENST00000448276.7:c.395G= MANE Select ENSP00000392617.2:p.Arg132=
ENST00000225742.13:c.170G= ENSP00000225742.9:p.Arg57=
ENST00000323347.14:c.251G= ENSP00000318451.10:p.Arg84=
ENST00000448276.6:c.395G= ENSP00000392617.2:p.Arg132=
ENST00000577686.1:n.53-210G=
ENST00000580054.1:c.179G= ENSP00000463793.1:p.Arg60=
ENST00000584400.5:c.217-210G= ENSP00000464503.1:n.217-210G=
ENST00000613943.4:c.284G= ENSP00000483605.1:p.Arg95=
NM_001098426.1:c.395G= NP_001091896.1:p.Arg132=
XM_005257604.2:c.170G= XP_005257661.2:p.Arg57=
NM_001330439.1:c.170G= NP_001317368.1:p.Arg57=
NM_001330440.1:c.251G= NP_001317369.1:p.Arg84=
NM_001098426.2:c.395G= MANE Select NP_001091896.1:p.Arg132=
NM_001330440.2:c.251G= NP_001317369.1:p.Arg84=