Canonical Allele Identifier: CA2270103118

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832541A= , CM000679.2:g.63832541A=	GRCh38
NC_000017.10:g.61909901A= , CM000679.1:g.61909901A=	GRCh37
NC_000017.9:g.59263633A=	NCBI36
NG_053004.1:g.15451T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2272T=
ENST00000697953.1:n.2845T=
ENST00000698013.1:n.2957T=
ENST00000698014.1:n.3180T=
ENST00000698015.1:n.2273T=
ENST00000698016.1:c.*397T=	ENSP00000513502.1:n.*397T=
ENST00000698017.1:n.2347T=
ENST00000698018.1:n.2478T=
ENST00000698019.1:n.2676T=
ENST00000698020.1:n.1782T=
ENST00000698021.1:c.1691T=
ENST00000698022.1:c.*397T=	ENSP00000513504.1:n.*397T=
ENST00000698023.1:n.2376T=
ENST00000698024.1:n.2238T=
ENST00000698025.1:n.2398T=
ENST00000698026.1:n.1289T=
ENST00000698027.1:c.*614T=	ENSP00000513505.1:n.*614T=
ENST00000698028.1:n.2481T=
ENST00000698029.1:n.3210T=
ENST00000448276.7:c.*397T= MANE Select	ENSP00000392617.2:n.*397T=
ENST00000323347.14:c.*397T=	ENSP00000318451.10:n.*397T=
ENST00000448276.6:c.*397T=	ENSP00000392617.2:n.*397T=
ENST00000613943.4:c.1882T=	ENSP00000483605.1:n.1882T=
NM_001098426.1:c.*397T=	NP_001091896.1:n.*397T=
XM_005257604.2:c.*397T=	XP_005257661.2:n.*397T=
NM_001330439.1:c.*397T=	NP_001317368.1:n.*397T=
NM_001330440.1:c.*397T=	NP_001317369.1:n.*397T=
NM_001098426.2:c.*397T= MANE Select	NP_001091896.1:n.*397T=
NM_001330440.2:c.*397T=	NP_001317369.1:n.*397T=