Canonical Allele Identifier: CA2810124116

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832558T>A , CM000679.2:g.63832558T>A	GRCh38
NC_000017.10:g.61909918T>A , CM000679.1:g.61909918T>A	GRCh37
NC_000017.9:g.59263650T>A	NCBI36
NG_053004.1:g.15434A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2255A>T
ENST00000697953.1:n.2828A>T
ENST00000698013.1:n.2940A>T
ENST00000698014.1:n.3163A>T
ENST00000698015.1:n.2256A>T
ENST00000698016.1:c.*380A>T	ENSP00000513502.1:n.*380A>T
ENST00000698017.1:n.2330A>T
ENST00000698018.1:n.2461A>T
ENST00000698019.1:n.2659A>T
ENST00000698020.1:n.1765A>T
ENST00000698021.1:c.1674A>T
ENST00000698022.1:c.*380A>T	ENSP00000513504.1:n.*380A>T
ENST00000698023.1:n.2359A>T
ENST00000698024.1:n.2221A>T
ENST00000698025.1:n.2381A>T
ENST00000698026.1:n.1272A>T
ENST00000698027.1:c.*597A>T	ENSP00000513505.1:n.*597A>T
ENST00000698028.1:n.2464A>T
ENST00000698029.1:n.3193A>T
ENST00000448276.7:c.*380A>T MANE Select	ENSP00000392617.2:n.*380A>T
ENST00000323347.14:c.*380A>T	ENSP00000318451.10:n.*380A>T
ENST00000448276.6:c.*380A>T	ENSP00000392617.2:n.*380A>T
ENST00000613943.4:c.1865A>T	ENSP00000483605.1:n.1865A>T
NM_001098426.1:c.*380A>T	NP_001091896.1:n.*380A>T
XM_005257604.2:c.*380A>T	XP_005257661.2:n.*380A>T
NM_001330439.1:c.*380A>T	NP_001317368.1:n.*380A>T
NM_001330440.1:c.*380A>T	NP_001317369.1:n.*380A>T
NM_001098426.2:c.*380A>T MANE Select	NP_001091896.1:n.*380A>T
NM_001330440.2:c.*380A>T	NP_001317369.1:n.*380A>T