Canonical Allele Identifier: CA2270103369

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832338G= , CM000679.2:g.63832338G=	GRCh38
NC_000017.10:g.61909698G= , CM000679.1:g.61909698G=	GRCh37
NC_000017.9:g.59263430G=	NCBI36
NG_053004.1:g.15654C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2475C=
ENST00000697953.1:n.3048C=
ENST00000698013.1:n.3160C=
ENST00000698014.1:n.3383C=
ENST00000698015.1:n.2476C=
ENST00000698016.1:c.*600C=	ENSP00000513502.1:n.*600C=
ENST00000698017.1:n.2550C=
ENST00000698018.1:n.2681C=
ENST00000698019.1:n.2879C=
ENST00000698020.1:n.1985C=
ENST00000698021.1:c.1894C=
ENST00000698022.1:c.*600C=	ENSP00000513504.1:n.*600C=
ENST00000698023.1:n.2579C=
ENST00000698024.1:n.2441C=
ENST00000698025.1:n.2601C=
ENST00000698026.1:n.1492C=
ENST00000698027.1:c.*817C=	ENSP00000513505.1:n.*817C=
ENST00000698028.1:n.2684C=
ENST00000698029.1:n.3413C=
ENST00000448276.7:c.*600C= MANE Select	ENSP00000392617.2:n.*600C=
ENST00000448276.6:c.*600C=	ENSP00000392617.2:n.*600C=
ENST00000613943.4:c.2085C=	ENSP00000483605.1:n.2085C=
NM_001098426.1:c.*600C=	NP_001091896.1:n.*600C=
XM_005257604.2:c.*600C=	XP_005257661.2:n.*600C=
NM_001330439.1:c.*600C=	NP_001317368.1:n.*600C=
NM_001330440.1:c.*600C=	NP_001317369.1:n.*600C=
NM_001098426.2:c.*600C= MANE Select	NP_001091896.1:n.*600C=
NM_001330440.2:c.*600C=	NP_001317369.1:n.*600C=