Canonical Allele Identifier: CA2270103044

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832180A= , CM000679.2:g.63832180A=	GRCh38
NC_000017.10:g.61909540A= , CM000679.1:g.61909540A=	GRCh37
NC_000017.9:g.59263272A=	NCBI36
NG_053004.1:g.15812T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2633T=
ENST00000697953.1:n.3206T=
ENST00000698013.1:n.3318T=
ENST00000698014.1:n.3541T=
ENST00000698015.1:n.2634T=
ENST00000698016.1:c.*758T=	ENSP00000513502.1:n.*758T=
ENST00000698017.1:n.2708T=
ENST00000698018.1:n.2839T=
ENST00000698019.1:n.3037T=
ENST00000698020.1:n.2143T=
ENST00000698021.1:c.2052T=
ENST00000698022.1:c.*758T=	ENSP00000513504.1:n.*758T=
ENST00000698023.1:n.2737T=
ENST00000698024.1:n.2599T=
ENST00000698025.1:n.2759T=
ENST00000698026.1:n.1650T=
ENST00000698027.1:c.*975T=	ENSP00000513505.1:n.*975T=
ENST00000448276.7:c.*758T= MANE Select	ENSP00000392617.2:n.*758T=
ENST00000448276.6:c.*758T=	ENSP00000392617.2:n.*758T=
ENST00000613943.4:c.2243T=	ENSP00000483605.1:n.2243T=
NM_001098426.1:c.*758T=	NP_001091896.1:n.*758T=
XM_005257604.2:c.*758T=	XP_005257661.2:n.*758T=
NM_001330439.1:c.*758T=	NP_001317368.1:n.*758T=
NM_001330440.1:c.*758T=	NP_001317369.1:n.*758T=
NM_001098426.2:c.*758T= MANE Select	NP_001091896.1:n.*758T=
NM_001330440.2:c.*758T=	NP_001317369.1:n.*758T=