Canonical Allele Identifier: CA2270103347

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832317G= , CM000679.2:g.63832317G=	GRCh38
NC_000017.10:g.61909677G= , CM000679.1:g.61909677G=	GRCh37
NC_000017.9:g.59263409G=	NCBI36
NG_053004.1:g.15675C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2496C=
ENST00000697953.1:n.3069C=
ENST00000698013.1:n.3181C=
ENST00000698014.1:n.3404C=
ENST00000698015.1:n.2497C=
ENST00000698016.1:c.*621C=	ENSP00000513502.1:n.*621C=
ENST00000698017.1:n.2571C=
ENST00000698018.1:n.2702C=
ENST00000698019.1:n.2900C=
ENST00000698020.1:n.2006C=
ENST00000698021.1:c.1915C=
ENST00000698022.1:c.*621C=	ENSP00000513504.1:n.*621C=
ENST00000698023.1:n.2600C=
ENST00000698024.1:n.2462C=
ENST00000698025.1:n.2622C=
ENST00000698026.1:n.1513C=
ENST00000698027.1:c.*838C=	ENSP00000513505.1:n.*838C=
ENST00000698028.1:n.2705C=
ENST00000698029.1:n.3434C=
ENST00000448276.7:c.*621C= MANE Select	ENSP00000392617.2:n.*621C=
ENST00000448276.6:c.*621C=	ENSP00000392617.2:n.*621C=
ENST00000613943.4:c.2106C=	ENSP00000483605.1:n.2106C=
NM_001098426.1:c.*621C=	NP_001091896.1:n.*621C=
XM_005257604.2:c.*621C=	XP_005257661.2:n.*621C=
NM_001330439.1:c.*621C=	NP_001317368.1:n.*621C=
NM_001330440.1:c.*621C=	NP_001317369.1:n.*621C=
NM_001098426.2:c.*621C= MANE Select	NP_001091896.1:n.*621C=
NM_001330440.2:c.*621C=	NP_001317369.1:n.*621C=