Canonical Allele Identifier: CA2270103101

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832489C= , CM000679.2:g.63832489C=	GRCh38
NC_000017.10:g.61909849C= , CM000679.1:g.61909849C=	GRCh37
NC_000017.9:g.59263581C=	NCBI36
NG_053004.1:g.15503G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2324G=
ENST00000697953.1:n.2897G=
ENST00000698013.1:n.3009G=
ENST00000698014.1:n.3232G=
ENST00000698015.1:n.2325G=
ENST00000698016.1:c.*449G=	ENSP00000513502.1:n.*449G=
ENST00000698017.1:n.2399G=
ENST00000698018.1:n.2530G=
ENST00000698019.1:n.2728G=
ENST00000698020.1:n.1834G=
ENST00000698021.1:c.1743G=
ENST00000698022.1:c.*449G=	ENSP00000513504.1:n.*449G=
ENST00000698023.1:n.2428G=
ENST00000698024.1:n.2290G=
ENST00000698025.1:n.2450G=
ENST00000698026.1:n.1341G=
ENST00000698027.1:c.*666G=	ENSP00000513505.1:n.*666G=
ENST00000698028.1:n.2533G=
ENST00000698029.1:n.3262G=
ENST00000448276.7:c.*449G= MANE Select	ENSP00000392617.2:n.*449G=
ENST00000448276.6:c.*449G=	ENSP00000392617.2:n.*449G=
ENST00000613943.4:c.1934G=	ENSP00000483605.1:n.1934G=
NM_001098426.1:c.*449G=	NP_001091896.1:n.*449G=
XM_005257604.2:c.*449G=	XP_005257661.2:n.*449G=
NM_001330439.1:c.*449G=	NP_001317368.1:n.*449G=
NM_001330440.1:c.*449G=	NP_001317369.1:n.*449G=
NM_001098426.2:c.*449G= MANE Select	NP_001091896.1:n.*449G=
NM_001330440.2:c.*449G=	NP_001317369.1:n.*449G=