Canonical Allele Identifier: CA2270103419

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832389A= , CM000679.2:g.63832389A=	GRCh38
NC_000017.10:g.61909749A= , CM000679.1:g.61909749A=	GRCh37
NC_000017.9:g.59263481A=	NCBI36
NG_053004.1:g.15603T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2424T=
ENST00000697953.1:n.2997T=
ENST00000698013.1:n.3109T=
ENST00000698014.1:n.3332T=
ENST00000698015.1:n.2425T=
ENST00000698016.1:c.*549T=	ENSP00000513502.1:n.*549T=
ENST00000698017.1:n.2499T=
ENST00000698018.1:n.2630T=
ENST00000698019.1:n.2828T=
ENST00000698020.1:n.1934T=
ENST00000698021.1:c.1843T=
ENST00000698022.1:c.*549T=	ENSP00000513504.1:n.*549T=
ENST00000698023.1:n.2528T=
ENST00000698024.1:n.2390T=
ENST00000698025.1:n.2550T=
ENST00000698026.1:n.1441T=
ENST00000698027.1:c.*766T=	ENSP00000513505.1:n.*766T=
ENST00000698028.1:n.2633T=
ENST00000698029.1:n.3362T=
ENST00000448276.7:c.*549T= MANE Select	ENSP00000392617.2:n.*549T=
ENST00000448276.6:c.*549T=	ENSP00000392617.2:n.*549T=
ENST00000613943.4:c.2034T=	ENSP00000483605.1:n.2034T=
NM_001098426.1:c.*549T=	NP_001091896.1:n.*549T=
XM_005257604.2:c.*549T=	XP_005257661.2:n.*549T=
NM_001330439.1:c.*549T=	NP_001317368.1:n.*549T=
NM_001330440.1:c.*549T=	NP_001317369.1:n.*549T=
NM_001098426.2:c.*549T= MANE Select	NP_001091896.1:n.*549T=
NM_001330440.2:c.*549T=	NP_001317369.1:n.*549T=