Canonical Allele Identifier: CA2270103075

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832442G= , CM000679.2:g.63832442G=	GRCh38
NC_000017.10:g.61909802G= , CM000679.1:g.61909802G=	GRCh37
NC_000017.9:g.59263534G=	NCBI36
NG_053004.1:g.15550C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2371C=
ENST00000697953.1:n.2944C=
ENST00000698013.1:n.3056C=
ENST00000698014.1:n.3279C=
ENST00000698015.1:n.2372C=
ENST00000698016.1:c.*496C=	ENSP00000513502.1:n.*496C=
ENST00000698017.1:n.2446C=
ENST00000698018.1:n.2577C=
ENST00000698019.1:n.2775C=
ENST00000698020.1:n.1881C=
ENST00000698021.1:c.1790C=
ENST00000698022.1:c.*496C=	ENSP00000513504.1:n.*496C=
ENST00000698023.1:n.2475C=
ENST00000698024.1:n.2337C=
ENST00000698025.1:n.2497C=
ENST00000698026.1:n.1388C=
ENST00000698027.1:c.*713C=	ENSP00000513505.1:n.*713C=
ENST00000698028.1:n.2580C=
ENST00000698029.1:n.3309C=
ENST00000448276.7:c.*496C= MANE Select	ENSP00000392617.2:n.*496C=
ENST00000448276.6:c.*496C=	ENSP00000392617.2:n.*496C=
ENST00000613943.4:c.1981C=	ENSP00000483605.1:n.1981C=
NM_001098426.1:c.*496C=	NP_001091896.1:n.*496C=
XM_005257604.2:c.*496C=	XP_005257661.2:n.*496C=
NM_001330439.1:c.*496C=	NP_001317368.1:n.*496C=
NM_001330440.1:c.*496C=	NP_001317369.1:n.*496C=
NM_001098426.2:c.*496C= MANE Select	NP_001091896.1:n.*496C=
NM_001330440.2:c.*496C=	NP_001317369.1:n.*496C=