Canonical Allele Identifier: CA2270103117

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832539G= , CM000679.2:g.63832539G=	GRCh38
NC_000017.10:g.61909899G= , CM000679.1:g.61909899G=	GRCh37
NC_000017.9:g.59263631G=	NCBI36
NG_053004.1:g.15453C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2274C=
ENST00000697953.1:n.2847C=
ENST00000698013.1:n.2959C=
ENST00000698014.1:n.3182C=
ENST00000698015.1:n.2275C=
ENST00000698016.1:c.*399C=	ENSP00000513502.1:n.*399C=
ENST00000698017.1:n.2349C=
ENST00000698018.1:n.2480C=
ENST00000698019.1:n.2678C=
ENST00000698020.1:n.1784C=
ENST00000698021.1:c.1693C=
ENST00000698022.1:c.*399C=	ENSP00000513504.1:n.*399C=
ENST00000698023.1:n.2378C=
ENST00000698024.1:n.2240C=
ENST00000698025.1:n.2400C=
ENST00000698026.1:n.1291C=
ENST00000698027.1:c.*616C=	ENSP00000513505.1:n.*616C=
ENST00000698028.1:n.2483C=
ENST00000698029.1:n.3212C=
ENST00000448276.7:c.*399C= MANE Select	ENSP00000392617.2:n.*399C=
ENST00000323347.14:c.*399C=	ENSP00000318451.10:n.*399C=
ENST00000448276.6:c.*399C=	ENSP00000392617.2:n.*399C=
ENST00000613943.4:c.1884C=	ENSP00000483605.1:n.1884C=
NM_001098426.1:c.*399C=	NP_001091896.1:n.*399C=
XM_005257604.2:c.*399C=	XP_005257661.2:n.*399C=
NM_001330439.1:c.*399C=	NP_001317368.1:n.*399C=
NM_001330440.1:c.*399C=	NP_001317369.1:n.*399C=
NM_001098426.2:c.*399C= MANE Select	NP_001091896.1:n.*399C=
NM_001330440.2:c.*399C=	NP_001317369.1:n.*399C=