Canonical Allele Identifier: CA2270103181

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832221C= , CM000679.2:g.63832221C=	GRCh38
NC_000017.10:g.61909581C= , CM000679.1:g.61909581C=	GRCh37
NC_000017.9:g.59263313C=	NCBI36
NG_053004.1:g.15771G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2592G=
ENST00000697953.1:n.3165G=
ENST00000698013.1:n.3277G=
ENST00000698014.1:n.3500G=
ENST00000698015.1:n.2593G=
ENST00000698016.1:c.*717G=	ENSP00000513502.1:n.*717G=
ENST00000698017.1:n.2667G=
ENST00000698018.1:n.2798G=
ENST00000698019.1:n.2996G=
ENST00000698020.1:n.2102G=
ENST00000698021.1:c.2011G=
ENST00000698022.1:c.*717G=	ENSP00000513504.1:n.*717G=
ENST00000698023.1:n.2696G=
ENST00000698024.1:n.2558G=
ENST00000698025.1:n.2718G=
ENST00000698026.1:n.1609G=
ENST00000698027.1:c.*934G=	ENSP00000513505.1:n.*934G=
ENST00000698028.1:n.2801G=
ENST00000448276.7:c.*717G= MANE Select	ENSP00000392617.2:n.*717G=
ENST00000448276.6:c.*717G=	ENSP00000392617.2:n.*717G=
ENST00000613943.4:c.2202G=	ENSP00000483605.1:n.2202G=
NM_001098426.1:c.*717G=	NP_001091896.1:n.*717G=
XM_005257604.2:c.*717G=	XP_005257661.2:n.*717G=
NM_001330439.1:c.*717G=	NP_001317368.1:n.*717G=
NM_001330440.1:c.*717G=	NP_001317369.1:n.*717G=
NM_001098426.2:c.*717G= MANE Select	NP_001091896.1:n.*717G=
NM_001330440.2:c.*717G=	NP_001317369.1:n.*717G=