Canonical Allele Identifier: CA2270103093

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832474G= , CM000679.2:g.63832474G=	GRCh38
NC_000017.10:g.61909834G= , CM000679.1:g.61909834G=	GRCh37
NC_000017.9:g.59263566G=	NCBI36
NG_053004.1:g.15518C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2339C=
ENST00000697953.1:n.2912C=
ENST00000698013.1:n.3024C=
ENST00000698014.1:n.3247C=
ENST00000698015.1:n.2340C=
ENST00000698016.1:c.*464C=	ENSP00000513502.1:n.*464C=
ENST00000698017.1:n.2414C=
ENST00000698018.1:n.2545C=
ENST00000698019.1:n.2743C=
ENST00000698020.1:n.1849C=
ENST00000698021.1:c.1758C=
ENST00000698022.1:c.*464C=	ENSP00000513504.1:n.*464C=
ENST00000698023.1:n.2443C=
ENST00000698024.1:n.2305C=
ENST00000698025.1:n.2465C=
ENST00000698026.1:n.1356C=
ENST00000698027.1:c.*681C=	ENSP00000513505.1:n.*681C=
ENST00000698028.1:n.2548C=
ENST00000698029.1:n.3277C=
ENST00000448276.7:c.*464C= MANE Select	ENSP00000392617.2:n.*464C=
ENST00000448276.6:c.*464C=	ENSP00000392617.2:n.*464C=
ENST00000613943.4:c.1949C=	ENSP00000483605.1:n.1949C=
NM_001098426.1:c.*464C=	NP_001091896.1:n.*464C=
XM_005257604.2:c.*464C=	XP_005257661.2:n.*464C=
NM_001330439.1:c.*464C=	NP_001317368.1:n.*464C=
NM_001330440.1:c.*464C=	NP_001317369.1:n.*464C=
NM_001098426.2:c.*464C= MANE Select	NP_001091896.1:n.*464C=
NM_001330440.2:c.*464C=	NP_001317369.1:n.*464C=