Canonical Allele Identifier: CA2270103079

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832452T= , CM000679.2:g.63832452T=	GRCh38
NC_000017.10:g.61909812T= , CM000679.1:g.61909812T=	GRCh37
NC_000017.9:g.59263544T=	NCBI36
NG_053004.1:g.15540A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2361A=
ENST00000697953.1:n.2934A=
ENST00000698013.1:n.3046A=
ENST00000698014.1:n.3269A=
ENST00000698015.1:n.2362A=
ENST00000698016.1:c.*486A=	ENSP00000513502.1:n.*486A=
ENST00000698017.1:n.2436A=
ENST00000698018.1:n.2567A=
ENST00000698019.1:n.2765A=
ENST00000698020.1:n.1871A=
ENST00000698021.1:c.1780A=
ENST00000698022.1:c.*486A=	ENSP00000513504.1:n.*486A=
ENST00000698023.1:n.2465A=
ENST00000698024.1:n.2327A=
ENST00000698025.1:n.2487A=
ENST00000698026.1:n.1378A=
ENST00000698027.1:c.*703A=	ENSP00000513505.1:n.*703A=
ENST00000698028.1:n.2570A=
ENST00000698029.1:n.3299A=
ENST00000448276.7:c.*486A= MANE Select	ENSP00000392617.2:n.*486A=
ENST00000448276.6:c.*486A=	ENSP00000392617.2:n.*486A=
ENST00000613943.4:c.1971A=	ENSP00000483605.1:n.1971A=
NM_001098426.1:c.*486A=	NP_001091896.1:n.*486A=
XM_005257604.2:c.*486A=	XP_005257661.2:n.*486A=
NM_001330439.1:c.*486A=	NP_001317368.1:n.*486A=
NM_001330440.1:c.*486A=	NP_001317369.1:n.*486A=
NM_001098426.2:c.*486A= MANE Select	NP_001091896.1:n.*486A=
NM_001330440.2:c.*486A=	NP_001317369.1:n.*486A=