Canonical Allele Identifier: CA2270103115

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832529G= , CM000679.2:g.63832529G=	GRCh38
NC_000017.10:g.61909889G= , CM000679.1:g.61909889G=	GRCh37
NC_000017.9:g.59263621G=	NCBI36
NG_053004.1:g.15463C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2284C=
ENST00000697953.1:n.2857C=
ENST00000698013.1:n.2969C=
ENST00000698014.1:n.3192C=
ENST00000698015.1:n.2285C=
ENST00000698016.1:c.*409C=	ENSP00000513502.1:n.*409C=
ENST00000698017.1:n.2359C=
ENST00000698018.1:n.2490C=
ENST00000698019.1:n.2688C=
ENST00000698020.1:n.1794C=
ENST00000698021.1:c.1703C=
ENST00000698022.1:c.*409C=	ENSP00000513504.1:n.*409C=
ENST00000698023.1:n.2388C=
ENST00000698024.1:n.2250C=
ENST00000698025.1:n.2410C=
ENST00000698026.1:n.1301C=
ENST00000698027.1:c.*626C=	ENSP00000513505.1:n.*626C=
ENST00000698028.1:n.2493C=
ENST00000698029.1:n.3222C=
ENST00000448276.7:c.*409C= MANE Select	ENSP00000392617.2:n.*409C=
ENST00000323347.14:c.*409C=	ENSP00000318451.10:n.*409C=
ENST00000448276.6:c.*409C=	ENSP00000392617.2:n.*409C=
ENST00000613943.4:c.1894C=	ENSP00000483605.1:n.1894C=
NM_001098426.1:c.*409C=	NP_001091896.1:n.*409C=
XM_005257604.2:c.*409C=	XP_005257661.2:n.*409C=
NM_001330439.1:c.*409C=	NP_001317368.1:n.*409C=
NM_001330440.1:c.*409C=	NP_001317369.1:n.*409C=
NM_001098426.2:c.*409C= MANE Select	NP_001091896.1:n.*409C=
NM_001330440.2:c.*409C=	NP_001317369.1:n.*409C=