Canonical Allele Identifier: CA2270103114

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832521T= , CM000679.2:g.63832521T=	GRCh38
NC_000017.10:g.61909881T= , CM000679.1:g.61909881T=	GRCh37
NC_000017.9:g.59263613T=	NCBI36
NG_053004.1:g.15471A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2292A=
ENST00000697953.1:n.2865A=
ENST00000698013.1:n.2977A=
ENST00000698014.1:n.3200A=
ENST00000698015.1:n.2293A=
ENST00000698016.1:c.*417A=	ENSP00000513502.1:n.*417A=
ENST00000698017.1:n.2367A=
ENST00000698018.1:n.2498A=
ENST00000698019.1:n.2696A=
ENST00000698020.1:n.1802A=
ENST00000698021.1:c.1711A=
ENST00000698022.1:c.*417A=	ENSP00000513504.1:n.*417A=
ENST00000698023.1:n.2396A=
ENST00000698024.1:n.2258A=
ENST00000698025.1:n.2418A=
ENST00000698026.1:n.1309A=
ENST00000698027.1:c.*634A=	ENSP00000513505.1:n.*634A=
ENST00000698028.1:n.2501A=
ENST00000698029.1:n.3230A=
ENST00000448276.7:c.*417A= MANE Select	ENSP00000392617.2:n.*417A=
ENST00000323347.14:c.*417A=	ENSP00000318451.10:n.*417A=
ENST00000448276.6:c.*417A=	ENSP00000392617.2:n.*417A=
ENST00000613943.4:c.1902A=	ENSP00000483605.1:n.1902A=
NM_001098426.1:c.*417A=	NP_001091896.1:n.*417A=
XM_005257604.2:c.*417A=	XP_005257661.2:n.*417A=
NM_001330439.1:c.*417A=	NP_001317368.1:n.*417A=
NM_001330440.1:c.*417A=	NP_001317369.1:n.*417A=
NM_001098426.2:c.*417A= MANE Select	NP_001091896.1:n.*417A=
NM_001330440.2:c.*417A=	NP_001317369.1:n.*417A=