Canonical Allele Identifier: CA2270103110

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832517A= , CM000679.2:g.63832517A=	GRCh38
NC_000017.10:g.61909877A= , CM000679.1:g.61909877A=	GRCh37
NC_000017.9:g.59263609A=	NCBI36
NG_053004.1:g.15475T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2296T=
ENST00000697953.1:n.2869T=
ENST00000698013.1:n.2981T=
ENST00000698014.1:n.3204T=
ENST00000698015.1:n.2297T=
ENST00000698016.1:c.*421T=	ENSP00000513502.1:n.*421T=
ENST00000698017.1:n.2371T=
ENST00000698018.1:n.2502T=
ENST00000698019.1:n.2700T=
ENST00000698020.1:n.1806T=
ENST00000698021.1:c.1715T=
ENST00000698022.1:c.*421T=	ENSP00000513504.1:n.*421T=
ENST00000698023.1:n.2400T=
ENST00000698024.1:n.2262T=
ENST00000698025.1:n.2422T=
ENST00000698026.1:n.1313T=
ENST00000698027.1:c.*638T=	ENSP00000513505.1:n.*638T=
ENST00000698028.1:n.2505T=
ENST00000698029.1:n.3234T=
ENST00000448276.7:c.*421T= MANE Select	ENSP00000392617.2:n.*421T=
ENST00000323347.14:c.*421T=	ENSP00000318451.10:n.*421T=
ENST00000448276.6:c.*421T=	ENSP00000392617.2:n.*421T=
ENST00000613943.4:c.1906T=	ENSP00000483605.1:n.1906T=
NM_001098426.1:c.*421T=	NP_001091896.1:n.*421T=
XM_005257604.2:c.*421T=	XP_005257661.2:n.*421T=
NM_001330439.1:c.*421T=	NP_001317368.1:n.*421T=
NM_001330440.1:c.*421T=	NP_001317369.1:n.*421T=
NM_001098426.2:c.*421T= MANE Select	NP_001091896.1:n.*421T=
NM_001330440.2:c.*421T=	NP_001317369.1:n.*421T=