Canonical Allele Identifier: CA2270103095

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832475G= , CM000679.2:g.63832475G=	GRCh38
NC_000017.10:g.61909835G= , CM000679.1:g.61909835G=	GRCh37
NC_000017.9:g.59263567G=	NCBI36
NG_053004.1:g.15517C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2338C=
ENST00000697953.1:n.2911C=
ENST00000698013.1:n.3023C=
ENST00000698014.1:n.3246C=
ENST00000698015.1:n.2339C=
ENST00000698016.1:c.*463C=	ENSP00000513502.1:n.*463C=
ENST00000698017.1:n.2413C=
ENST00000698018.1:n.2544C=
ENST00000698019.1:n.2742C=
ENST00000698020.1:n.1848C=
ENST00000698021.1:c.1757C=
ENST00000698022.1:c.*463C=	ENSP00000513504.1:n.*463C=
ENST00000698023.1:n.2442C=
ENST00000698024.1:n.2304C=
ENST00000698025.1:n.2464C=
ENST00000698026.1:n.1355C=
ENST00000698027.1:c.*680C=	ENSP00000513505.1:n.*680C=
ENST00000698028.1:n.2547C=
ENST00000698029.1:n.3276C=
ENST00000448276.7:c.*463C= MANE Select	ENSP00000392617.2:n.*463C=
ENST00000448276.6:c.*463C=	ENSP00000392617.2:n.*463C=
ENST00000613943.4:c.1948C=	ENSP00000483605.1:n.1948C=
NM_001098426.1:c.*463C=	NP_001091896.1:n.*463C=
XM_005257604.2:c.*463C=	XP_005257661.2:n.*463C=
NM_001330439.1:c.*463C=	NP_001317368.1:n.*463C=
NM_001330440.1:c.*463C=	NP_001317369.1:n.*463C=
NM_001098426.2:c.*463C= MANE Select	NP_001091896.1:n.*463C=
NM_001330440.2:c.*463C=	NP_001317369.1:n.*463C=