Canonical Allele Identifier: CA2270105536
Gene: SMARCD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63837445G= , CM000679.2:g.63837445G= GRCh38
NC_000017.10:g.61914805G= , CM000679.1:g.61914805G= GRCh37
NC_000017.9:g.59268537G= NCBI36
NG_053004.1:g.10547C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697953.1:n.285C=
ENST00000698015.1:n.31C=
ENST00000698016.1:c.256C= ENSP00000513502.1:p.Arg86=
ENST00000698021.1:c.60C=
ENST00000698022.1:c.214C= ENSP00000513504.1:p.Arg72=
ENST00000698027.1:c.256C= ENSP00000513505.1:p.Arg86=
ENST00000448276.7:c.397C= MANE Select ENSP00000392617.2:p.Arg133=
ENST00000225742.13:c.172C= ENSP00000225742.9:p.Arg58=
ENST00000323347.14:c.253C= ENSP00000318451.10:p.Arg85=
ENST00000448276.6:c.397C= ENSP00000392617.2:p.Arg133=
ENST00000577686.1:n.53-208C=
ENST00000580054.1:c.181C= ENSP00000463793.1:p.Arg61=
ENST00000584400.5:c.217-208C= ENSP00000464503.1:n.217-208C=
ENST00000613943.4:c.286C= ENSP00000483605.1:p.Arg96=
NM_001098426.1:c.397C= NP_001091896.1:p.Arg133=
XM_005257604.2:c.172C= XP_005257661.2:p.Arg58=
NM_001330439.1:c.172C= NP_001317368.1:p.Arg58=
NM_001330440.1:c.253C= NP_001317369.1:p.Arg85=
NM_001098426.2:c.397C= MANE Select NP_001091896.1:p.Arg133=
NM_001330440.2:c.253C= NP_001317369.1:p.Arg85=