Canonical Allele Identifier: CA2270103024

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832139A= , CM000679.2:g.63832139A=	GRCh38
NC_000017.10:g.61909499A= , CM000679.1:g.61909499A=	GRCh37
NC_000017.9:g.59263231A=	NCBI36
NG_053004.1:g.15853T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.3247T=
ENST00000698013.1:n.3359T=
ENST00000698014.1:n.3582T=
ENST00000698015.1:n.2675T=
ENST00000698016.1:c.*799T=	ENSP00000513502.1:n.*799T=
ENST00000698017.1:n.2749T=
ENST00000698018.1:n.2880T=
ENST00000698019.1:n.3078T=
ENST00000698020.1:n.2184T=
ENST00000698021.1:c.2093T=
ENST00000698022.1:c.*799T=	ENSP00000513504.1:n.*799T=
ENST00000698023.1:n.2778T=
ENST00000698024.1:n.2640T=
ENST00000698025.1:n.2800T=
ENST00000698026.1:n.1691T=
ENST00000698027.1:c.*1016T=	ENSP00000513505.1:n.*1016T=
ENST00000448276.7:c.*799T= MANE Select	ENSP00000392617.2:n.*799T=
ENST00000448276.6:c.*799T=	ENSP00000392617.2:n.*799T=
ENST00000613943.4:c.2284T=	ENSP00000483605.1:n.2284T=
NM_001098426.1:c.*799T=	NP_001091896.1:n.*799T=
XM_005257604.2:c.*799T=	XP_005257661.2:n.*799T=
NM_001330439.1:c.*799T=	NP_001317368.1:n.*799T=
NM_001330440.1:c.*799T=	NP_001317369.1:n.*799T=
NM_001098426.2:c.*799T= MANE Select	NP_001091896.1:n.*799T=
NM_001330440.2:c.*799T=	NP_001317369.1:n.*799T=