Canonical Allele Identifier: CA773993004

Gene: SMARCD2

Linked Data

• dbSNP Id: rs1301230184
• MyVariant Identifiers: chr17:g.61909574_61909575insG (hg19) ; chr17:g.63832214_63832215insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832216dup , CM000679.2:g.63832216dup	GRCh38
NC_000017.10:g.61909576dup , CM000679.1:g.61909576dup	GRCh37
NC_000017.9:g.59263308dup	NCBI36
NG_053004.1:g.15777dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2598dup
ENST00000697953.1:n.3171dup
ENST00000698013.1:n.3283dup
ENST00000698014.1:n.3506dup
ENST00000698015.1:n.2599dup
ENST00000698016.1:c.*723dup	ENSP00000513502.1:n.*723dup
ENST00000698017.1:n.2673dup
ENST00000698018.1:n.2804dup
ENST00000698019.1:n.3002dup
ENST00000698020.1:n.2108dup
ENST00000698021.1:c.2017dup
ENST00000698022.1:c.*723dup	ENSP00000513504.1:n.*723dup
ENST00000698023.1:n.2702dup
ENST00000698024.1:n.2564dup
ENST00000698025.1:n.2724dup
ENST00000698026.1:n.1615dup
ENST00000698027.1:c.*940dup	ENSP00000513505.1:n.*940dup
ENST00000698028.1:n.2807dup
ENST00000448276.7:c.*723dup MANE Select	ENSP00000392617.2:n.*723dup
ENST00000448276.6:c.*723dup	ENSP00000392617.2:n.*723dup
ENST00000613943.4:c.2208dup	ENSP00000483605.1:n.2208dup
NM_001098426.1:c.*723dup	NP_001091896.1:n.*723dup
XM_005257604.2:c.*723dup	XP_005257661.2:n.*723dup
NM_001330439.1:c.*723dup	NP_001317368.1:n.*723dup
NM_001330440.1:c.*723dup	NP_001317369.1:n.*723dup
NM_001098426.2:c.*723dup MANE Select	NP_001091896.1:n.*723dup
NM_001330440.2:c.*723dup	NP_001317369.1:n.*723dup