Canonical Allele Identifier: CA2270103076

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832443C= , CM000679.2:g.63832443C=	GRCh38
NC_000017.10:g.61909803C= , CM000679.1:g.61909803C=	GRCh37
NC_000017.9:g.59263535C=	NCBI36
NG_053004.1:g.15549G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2370G=
ENST00000697953.1:n.2943G=
ENST00000698013.1:n.3055G=
ENST00000698014.1:n.3278G=
ENST00000698015.1:n.2371G=
ENST00000698016.1:c.*495G=	ENSP00000513502.1:n.*495G=
ENST00000698017.1:n.2445G=
ENST00000698018.1:n.2576G=
ENST00000698019.1:n.2774G=
ENST00000698020.1:n.1880G=
ENST00000698021.1:c.1789G=
ENST00000698022.1:c.*495G=	ENSP00000513504.1:n.*495G=
ENST00000698023.1:n.2474G=
ENST00000698024.1:n.2336G=
ENST00000698025.1:n.2496G=
ENST00000698026.1:n.1387G=
ENST00000698027.1:c.*712G=	ENSP00000513505.1:n.*712G=
ENST00000698028.1:n.2579G=
ENST00000698029.1:n.3308G=
ENST00000448276.7:c.*495G= MANE Select	ENSP00000392617.2:n.*495G=
ENST00000448276.6:c.*495G=	ENSP00000392617.2:n.*495G=
ENST00000613943.4:c.1980G=	ENSP00000483605.1:n.1980G=
NM_001098426.1:c.*495G=	NP_001091896.1:n.*495G=
XM_005257604.2:c.*495G=	XP_005257661.2:n.*495G=
NM_001330439.1:c.*495G=	NP_001317368.1:n.*495G=
NM_001330440.1:c.*495G=	NP_001317369.1:n.*495G=
NM_001098426.2:c.*495G= MANE Select	NP_001091896.1:n.*495G=
NM_001330440.2:c.*495G=	NP_001317369.1:n.*495G=