Canonical Allele Identifier: CA2270103342

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832313C= , CM000679.2:g.63832313C=	GRCh38
NC_000017.10:g.61909673C= , CM000679.1:g.61909673C=	GRCh37
NC_000017.9:g.59263405C=	NCBI36
NG_053004.1:g.15679G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2500G=
ENST00000697953.1:n.3073G=
ENST00000698013.1:n.3185G=
ENST00000698014.1:n.3408G=
ENST00000698015.1:n.2501G=
ENST00000698016.1:c.*625G=	ENSP00000513502.1:n.*625G=
ENST00000698017.1:n.2575G=
ENST00000698018.1:n.2706G=
ENST00000698019.1:n.2904G=
ENST00000698020.1:n.2010G=
ENST00000698021.1:c.1919G=
ENST00000698022.1:c.*625G=	ENSP00000513504.1:n.*625G=
ENST00000698023.1:n.2604G=
ENST00000698024.1:n.2466G=
ENST00000698025.1:n.2626G=
ENST00000698026.1:n.1517G=
ENST00000698027.1:c.*842G=	ENSP00000513505.1:n.*842G=
ENST00000698028.1:n.2709G=
ENST00000698029.1:n.3438G=
ENST00000448276.7:c.*625G= MANE Select	ENSP00000392617.2:n.*625G=
ENST00000448276.6:c.*625G=	ENSP00000392617.2:n.*625G=
ENST00000613943.4:c.2110G=	ENSP00000483605.1:n.2110G=
NM_001098426.1:c.*625G=	NP_001091896.1:n.*625G=
XM_005257604.2:c.*625G=	XP_005257661.2:n.*625G=
NM_001330439.1:c.*625G=	NP_001317368.1:n.*625G=
NM_001330440.1:c.*625G=	NP_001317369.1:n.*625G=
NM_001098426.2:c.*625G= MANE Select	NP_001091896.1:n.*625G=
NM_001330440.2:c.*625G=	NP_001317369.1:n.*625G=