Canonical Allele Identifier: CA2270103085

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832461T= , CM000679.2:g.63832461T=	GRCh38
NC_000017.10:g.61909821T= , CM000679.1:g.61909821T=	GRCh37
NC_000017.9:g.59263553T=	NCBI36
NG_053004.1:g.15531A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2352A=
ENST00000697953.1:n.2925A=
ENST00000698013.1:n.3037A=
ENST00000698014.1:n.3260A=
ENST00000698015.1:n.2353A=
ENST00000698016.1:c.*477A=	ENSP00000513502.1:n.*477A=
ENST00000698017.1:n.2427A=
ENST00000698018.1:n.2558A=
ENST00000698019.1:n.2756A=
ENST00000698020.1:n.1862A=
ENST00000698021.1:c.1771A=
ENST00000698022.1:c.*477A=	ENSP00000513504.1:n.*477A=
ENST00000698023.1:n.2456A=
ENST00000698024.1:n.2318A=
ENST00000698025.1:n.2478A=
ENST00000698026.1:n.1369A=
ENST00000698027.1:c.*694A=	ENSP00000513505.1:n.*694A=
ENST00000698028.1:n.2561A=
ENST00000698029.1:n.3290A=
ENST00000448276.7:c.*477A= MANE Select	ENSP00000392617.2:n.*477A=
ENST00000448276.6:c.*477A=	ENSP00000392617.2:n.*477A=
ENST00000613943.4:c.1962A=	ENSP00000483605.1:n.1962A=
NM_001098426.1:c.*477A=	NP_001091896.1:n.*477A=
XM_005257604.2:c.*477A=	XP_005257661.2:n.*477A=
NM_001330439.1:c.*477A=	NP_001317368.1:n.*477A=
NM_001330440.1:c.*477A=	NP_001317369.1:n.*477A=
NM_001098426.2:c.*477A= MANE Select	NP_001091896.1:n.*477A=
NM_001330440.2:c.*477A=	NP_001317369.1:n.*477A=