Canonical Allele Identifier: CA2270103078

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832446C= , CM000679.2:g.63832446C=	GRCh38
NC_000017.10:g.61909806C= , CM000679.1:g.61909806C=	GRCh37
NC_000017.9:g.59263538C=	NCBI36
NG_053004.1:g.15546G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2367G=
ENST00000697953.1:n.2940G=
ENST00000698013.1:n.3052G=
ENST00000698014.1:n.3275G=
ENST00000698015.1:n.2368G=
ENST00000698016.1:c.*492G=	ENSP00000513502.1:n.*492G=
ENST00000698017.1:n.2442G=
ENST00000698018.1:n.2573G=
ENST00000698019.1:n.2771G=
ENST00000698020.1:n.1877G=
ENST00000698021.1:c.1786G=
ENST00000698022.1:c.*492G=	ENSP00000513504.1:n.*492G=
ENST00000698023.1:n.2471G=
ENST00000698024.1:n.2333G=
ENST00000698025.1:n.2493G=
ENST00000698026.1:n.1384G=
ENST00000698027.1:c.*709G=	ENSP00000513505.1:n.*709G=
ENST00000698028.1:n.2576G=
ENST00000698029.1:n.3305G=
ENST00000448276.7:c.*492G= MANE Select	ENSP00000392617.2:n.*492G=
ENST00000448276.6:c.*492G=	ENSP00000392617.2:n.*492G=
ENST00000613943.4:c.1977G=	ENSP00000483605.1:n.1977G=
NM_001098426.1:c.*492G=	NP_001091896.1:n.*492G=
XM_005257604.2:c.*492G=	XP_005257661.2:n.*492G=
NM_001330439.1:c.*492G=	NP_001317368.1:n.*492G=
NM_001330440.1:c.*492G=	NP_001317369.1:n.*492G=
NM_001098426.2:c.*492G= MANE Select	NP_001091896.1:n.*492G=
NM_001330440.2:c.*492G=	NP_001317369.1:n.*492G=