Canonical Allele Identifier: CA2270103087

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832463C= , CM000679.2:g.63832463C=	GRCh38
NC_000017.10:g.61909823C= , CM000679.1:g.61909823C=	GRCh37
NC_000017.9:g.59263555C=	NCBI36
NG_053004.1:g.15529G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2350G=
ENST00000697953.1:n.2923G=
ENST00000698013.1:n.3035G=
ENST00000698014.1:n.3258G=
ENST00000698015.1:n.2351G=
ENST00000698016.1:c.*475G=	ENSP00000513502.1:n.*475G=
ENST00000698017.1:n.2425G=
ENST00000698018.1:n.2556G=
ENST00000698019.1:n.2754G=
ENST00000698020.1:n.1860G=
ENST00000698021.1:c.1769G=
ENST00000698022.1:c.*475G=	ENSP00000513504.1:n.*475G=
ENST00000698023.1:n.2454G=
ENST00000698024.1:n.2316G=
ENST00000698025.1:n.2476G=
ENST00000698026.1:n.1367G=
ENST00000698027.1:c.*692G=	ENSP00000513505.1:n.*692G=
ENST00000698028.1:n.2559G=
ENST00000698029.1:n.3288G=
ENST00000448276.7:c.*475G= MANE Select	ENSP00000392617.2:n.*475G=
ENST00000448276.6:c.*475G=	ENSP00000392617.2:n.*475G=
ENST00000613943.4:c.1960G=	ENSP00000483605.1:n.1960G=
NM_001098426.1:c.*475G=	NP_001091896.1:n.*475G=
XM_005257604.2:c.*475G=	XP_005257661.2:n.*475G=
NM_001330439.1:c.*475G=	NP_001317368.1:n.*475G=
NM_001330440.1:c.*475G=	NP_001317369.1:n.*475G=
NM_001098426.2:c.*475G= MANE Select	NP_001091896.1:n.*475G=
NM_001330440.2:c.*475G=	NP_001317369.1:n.*475G=