Canonical Allele Identifier: CA2270103127

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832557C= , CM000679.2:g.63832557C=	GRCh38
NC_000017.10:g.61909917C= , CM000679.1:g.61909917C=	GRCh37
NC_000017.9:g.59263649C=	NCBI36
NG_053004.1:g.15435G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2256G=
ENST00000697953.1:n.2829G=
ENST00000698013.1:n.2941G=
ENST00000698014.1:n.3164G=
ENST00000698015.1:n.2257G=
ENST00000698016.1:c.*381G=	ENSP00000513502.1:n.*381G=
ENST00000698017.1:n.2331G=
ENST00000698018.1:n.2462G=
ENST00000698019.1:n.2660G=
ENST00000698020.1:n.1766G=
ENST00000698021.1:c.1675G=
ENST00000698022.1:c.*381G=	ENSP00000513504.1:n.*381G=
ENST00000698023.1:n.2360G=
ENST00000698024.1:n.2222G=
ENST00000698025.1:n.2382G=
ENST00000698026.1:n.1273G=
ENST00000698027.1:c.*598G=	ENSP00000513505.1:n.*598G=
ENST00000698028.1:n.2465G=
ENST00000698029.1:n.3194G=
ENST00000448276.7:c.*381G= MANE Select	ENSP00000392617.2:n.*381G=
ENST00000323347.14:c.*381G=	ENSP00000318451.10:n.*381G=
ENST00000448276.6:c.*381G=	ENSP00000392617.2:n.*381G=
ENST00000613943.4:c.1866G=	ENSP00000483605.1:n.1866G=
NM_001098426.1:c.*381G=	NP_001091896.1:n.*381G=
XM_005257604.2:c.*381G=	XP_005257661.2:n.*381G=
NM_001330439.1:c.*381G=	NP_001317368.1:n.*381G=
NM_001330440.1:c.*381G=	NP_001317369.1:n.*381G=
NM_001098426.2:c.*381G= MANE Select	NP_001091896.1:n.*381G=
NM_001330440.2:c.*381G=	NP_001317369.1:n.*381G=