Canonical Allele Identifier: CA2270103387

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832354G= , CM000679.2:g.63832354G=	GRCh38
NC_000017.10:g.61909714G= , CM000679.1:g.61909714G=	GRCh37
NC_000017.9:g.59263446G=	NCBI36
NG_053004.1:g.15638C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2459C=
ENST00000697953.1:n.3032C=
ENST00000698013.1:n.3144C=
ENST00000698014.1:n.3367C=
ENST00000698015.1:n.2460C=
ENST00000698016.1:c.*584C=	ENSP00000513502.1:n.*584C=
ENST00000698017.1:n.2534C=
ENST00000698018.1:n.2665C=
ENST00000698019.1:n.2863C=
ENST00000698020.1:n.1969C=
ENST00000698021.1:c.1878C=
ENST00000698022.1:c.*584C=	ENSP00000513504.1:n.*584C=
ENST00000698023.1:n.2563C=
ENST00000698024.1:n.2425C=
ENST00000698025.1:n.2585C=
ENST00000698026.1:n.1476C=
ENST00000698027.1:c.*801C=	ENSP00000513505.1:n.*801C=
ENST00000698028.1:n.2668C=
ENST00000698029.1:n.3397C=
ENST00000448276.7:c.*584C= MANE Select	ENSP00000392617.2:n.*584C=
ENST00000448276.6:c.*584C=	ENSP00000392617.2:n.*584C=
ENST00000613943.4:c.2069C=	ENSP00000483605.1:n.2069C=
NM_001098426.1:c.*584C=	NP_001091896.1:n.*584C=
XM_005257604.2:c.*584C=	XP_005257661.2:n.*584C=
NM_001330439.1:c.*584C=	NP_001317368.1:n.*584C=
NM_001330440.1:c.*584C=	NP_001317369.1:n.*584C=
NM_001098426.2:c.*584C= MANE Select	NP_001091896.1:n.*584C=
NM_001330440.2:c.*584C=	NP_001317369.1:n.*584C=