Canonical Allele Identifier: CA2270103111

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832519C= , CM000679.2:g.63832519C=	GRCh38
NC_000017.10:g.61909879C= , CM000679.1:g.61909879C=	GRCh37
NC_000017.9:g.59263611C=	NCBI36
NG_053004.1:g.15473G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2294G=
ENST00000697953.1:n.2867G=
ENST00000698013.1:n.2979G=
ENST00000698014.1:n.3202G=
ENST00000698015.1:n.2295G=
ENST00000698016.1:c.*419G=	ENSP00000513502.1:n.*419G=
ENST00000698017.1:n.2369G=
ENST00000698018.1:n.2500G=
ENST00000698019.1:n.2698G=
ENST00000698020.1:n.1804G=
ENST00000698021.1:c.1713G=
ENST00000698022.1:c.*419G=	ENSP00000513504.1:n.*419G=
ENST00000698023.1:n.2398G=
ENST00000698024.1:n.2260G=
ENST00000698025.1:n.2420G=
ENST00000698026.1:n.1311G=
ENST00000698027.1:c.*636G=	ENSP00000513505.1:n.*636G=
ENST00000698028.1:n.2503G=
ENST00000698029.1:n.3232G=
ENST00000448276.7:c.*419G= MANE Select	ENSP00000392617.2:n.*419G=
ENST00000323347.14:c.*419G=	ENSP00000318451.10:n.*419G=
ENST00000448276.6:c.*419G=	ENSP00000392617.2:n.*419G=
ENST00000613943.4:c.1904G=	ENSP00000483605.1:n.1904G=
NM_001098426.1:c.*419G=	NP_001091896.1:n.*419G=
XM_005257604.2:c.*419G=	XP_005257661.2:n.*419G=
NM_001330439.1:c.*419G=	NP_001317368.1:n.*419G=
NM_001330440.1:c.*419G=	NP_001317369.1:n.*419G=
NM_001098426.2:c.*419G= MANE Select	NP_001091896.1:n.*419G=
NM_001330440.2:c.*419G=	NP_001317369.1:n.*419G=