Canonical Allele Identifier: CA2270103098

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832484_63832495delinsAGCAGCAAGGCT , CM000679.2:g.63832484_63832495delinsAGCAGCAAGGCT	GRCh38
NC_000017.10:g.61909844_61909855delinsAGCAGCAAGGCT , CM000679.1:g.61909844_61909855delinsAGCAGCAAGGCT	GRCh37
NC_000017.9:g.59263576_59263587delinsAGCAGCAAGGCT	NCBI36
NG_053004.1:g.15497_15508delinsAGCCTTGCTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2318_2329delinsAGCCTTGCTGCT
ENST00000697953.1:n.2891_2902delinsAGCCTTGCTGCT
ENST00000698013.1:n.3003_3014delinsAGCCTTGCTGCT
ENST00000698014.1:n.3226_3237delinsAGCCTTGCTGCT
ENST00000698015.1:n.2319_2330delinsAGCCTTGCTGCT
ENST00000698016.1:c.*443_*454delinsAGCCTTGCTGCT	ENSP00000513502.1:n.*443_*454delinsAGCCTTGCTGCT
ENST00000698017.1:n.2393_2404delinsAGCCTTGCTGCT
ENST00000698018.1:n.2524_2535delinsAGCCTTGCTGCT
ENST00000698019.1:n.2722_2733delinsAGCCTTGCTGCT
ENST00000698020.1:n.1828_1839delinsAGCCTTGCTGCT
ENST00000698021.1:c.1737_1748delinsAGCCTTGCTGCT
ENST00000698022.1:c.*443_*454delinsAGCCTTGCTGCT	ENSP00000513504.1:n.*443_*454delinsAGCCTTGCTGCT
ENST00000698023.1:n.2422_2433delinsAGCCTTGCTGCT
ENST00000698024.1:n.2284_2295delinsAGCCTTGCTGCT
ENST00000698025.1:n.2444_2455delinsAGCCTTGCTGCT
ENST00000698026.1:n.1335_1346delinsAGCCTTGCTGCT
ENST00000698027.1:c.*660_*671delinsAGCCTTGCTGCT	ENSP00000513505.1:n.*660_*671delinsAGCCTTGCTGCT
ENST00000698028.1:n.2527_2538delinsAGCCTTGCTGCT
ENST00000698029.1:n.3256_3267delinsAGCCTTGCTGCT
ENST00000448276.7:c.*443_*454delinsAGCCTTGCTGCT MANE Select	ENSP00000392617.2:n.*443_*454delinsAGCCTTGCTGCT
ENST00000448276.6:c.*443_*454delinsAGCCTTGCTGCT	ENSP00000392617.2:n.*443_*454delinsAGCCTTGCTGCT
ENST00000613943.4:c.1928_1939delinsAGCCTTGCTGCT	ENSP00000483605.1:n.1928_1939delinsAGCCTTGCTGCT
NM_001098426.1:c.*443_*454delinsAGCCTTGCTGCT	NP_001091896.1:n.*443_*454delinsAGCCTTGCTGCT
XM_005257604.2:c.*443_*454delinsAGCCTTGCTGCT	XP_005257661.2:n.*443_*454delinsAGCCTTGCTGCT
NM_001330439.1:c.*443_*454delinsAGCCTTGCTGCT	NP_001317368.1:n.*443_*454delinsAGCCTTGCTGCT
NM_001330440.1:c.*443_*454delinsAGCCTTGCTGCT	NP_001317369.1:n.*443_*454delinsAGCCTTGCTGCT
NM_001098426.2:c.*443_*454delinsAGCCTTGCTGCT MANE Select	NP_001091896.1:n.*443_*454delinsAGCCTTGCTGCT
NM_001330440.2:c.*443_*454delinsAGCCTTGCTGCT	NP_001317369.1:n.*443_*454delinsAGCCTTGCTGCT