Canonical Allele Identifier: CA1477545601

Gene: SMARCAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.94253666_94253678delinsGCACTGGTAAGTA , CM000666.2:g.94253666_94253678delinsGCACTGGTAAGTA	GRCh38
NC_000004.11:g.95174817_95174829delinsGCACTGGTAAGTA , CM000666.1:g.95174817_95174829delinsGCACTGGTAAGTA	GRCh37
NC_000004.10:g.95393840_95393852delinsGCACTGGTAAGTA	NCBI36
NG_031945.1:g.51059_51071delinsGCACTGGTAAGTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000354268.9:c.1281+659_1281+671delinsGCACTGGTAAGTA MANE Select	ENSP00000346217.4:n.1281+659_1281+671deli...
ENST00000354268.8:c.1281+659_1281+671delinsGCACTGGTAAGTA	ENSP00000346217.4:n.1281+659_1281+671deli...
ENST00000359052.8:c.1281+659_1281+671delinsGCACTGGTAAGTA	ENSP00000351947.4:n.1281+659_1281+671deli...
ENST00000394961.6:c.*1186+659_*1186+671delinsGCACTGGTAAGTA	ENSP00000378413.2:n.*1186+659_*1186+671de...
ENST00000457823.6:c.1281+659_1281+671delinsGCACTGGTAAGTA	ENSP00000415576.2:n.1281+659_1281+671deli...
ENST00000509418.1:c.-15_-10+7delinsGCACTGGTAAGTA
ENST00000510105.5:c.*619+659_*619+671delinsGCACTGGTAAGTA	ENSP00000424624.1:n.*619+659_*619+671deli...
NM_001128429.2:c.1281+659_1281+671delinsGCACTGGTAAGTA	NP_001121901.1:n.1281+659_1281+671delinsG...
NM_001128430.1:c.1281+659_1281+671delinsGCACTGGTAAGTA	NP_001121902.1:n.1281+659_1281+671delinsG...
NM_001254949.1:c.-15_-10+7delinsGCACTGGTAAGTA
NM_020159.4:c.1281+659_1281+671delinsGCACTGGTAAGTA	NP_064544.2:n.1281+659_1281+671delinsGCAC...
NR_045644.1:n.1607+659_1607+671delinsGCACTGGTAAGTA
XR_938765.1:n.1536+659_1536+671delinsGCACTGGTAAGTA
XR_938766.1:n.1536+659_1536+671delinsGCACTGGTAAGTA
XM_017008463.2:c.1281+659_1281+671delinsGCACTGGTAAGTA	XP_016863952.1:n.1281+659_1281+671delinsG...
XM_017008464.2:c.-466+659_-466+671delinsGCACTGGTAAGTA	XP_016863953.1:n.-466+659_-466+671delinsG...
XM_017008465.2:c.-466+659_-466+671delinsGCACTGGTAAGTA	XP_016863954.1:n.-466+659_-466+671delinsG...
XM_024454154.1:c.1281+659_1281+671delinsGCACTGGTAAGTA	XP_024309922.1:n.1281+659_1281+671delinsG...
XR_001741292.2:n.1458+659_1458+671delinsGCACTGGTAAGTA
XR_938765.2:n.1536+659_1536+671delinsGCACTGGTAAGTA
NM_001128429.3:c.1281+659_1281+671delinsGCACTGGTAAGTA	NP_001121901.1:n.1281+659_1281+671delinsG...
NM_001128430.2:c.1281+659_1281+671delinsGCACTGGTAAGTA	NP_001121902.1:n.1281+659_1281+671delinsG...
NM_001254949.2:c.-15_-10+7delinsGCACTGGTAAGTA
NM_001375855.1:c.1281+659_1281+671delinsGCACTGGTAAGTA	NP_001362784.1:n.1281+659_1281+671delinsG...
NM_001375856.1:c.1281+659_1281+671delinsGCACTGGTAAGTA	NP_001362785.1:n.1281+659_1281+671delinsG...
NM_001375857.1:c.1278+659_1278+671delinsGCACTGGTAAGTA	NP_001362786.1:n.1278+659_1278+671delinsG...
NM_001375858.1:c.1281+659_1281+671delinsGCACTGGTAAGTA	NP_001362787.1:n.1281+659_1281+671delinsG...
NM_001375859.1:c.-15_-10+7delinsGCACTGGTAAGTA
NM_020159.5:c.1281+659_1281+671delinsGCACTGGTAAGTA MANE Select	NP_064544.2:n.1281+659_1281+671delinsGCAC...
NR_045644.2:n.1607+659_1607+671delinsGCACTGGTAAGTA
NR_164722.1:n.1458+659_1458+671delinsGCACTGGTAAGTA
NR_164723.1:n.1536+659_1536+671delinsGCACTGGTAAGTA
NR_164724.1:n.1548+659_1548+671delinsGCACTGGTAAGTA
NR_164725.1:n.1458+659_1458+671delinsGCACTGGTAAGTA
NR_164726.1:n.1357+659_1357+671delinsGCACTGGTAAGTA
NR_164727.1:n.1533+659_1533+671delinsGCACTGGTAAGTA
NR_164728.1:n.1536+659_1536+671delinsGCACTGGTAAGTA
NR_164729.1:n.1458+659_1458+671delinsGCACTGGTAAGTA
NR_164730.1:n.1536+659_1536+671delinsGCACTGGTAAGTA
NR_164731.1:n.1533+659_1533+671delinsGCACTGGTAAGTA
NR_164732.1:n.1687+659_1687+671delinsGCACTGGTAAGTA
NR_164733.1:n.1536+659_1536+671delinsGCACTGGTAAGTA
NR_164734.1:n.1458+659_1458+671delinsGCACTGGTAAGTA
NR_164735.1:n.1357+659_1357+671delinsGCACTGGTAAGTA
NR_164736.1:n.1485+659_1485+671delinsGCACTGGTAAGTA
NR_164737.1:n.1626+659_1626+671delinsGCACTGGTAAGTA