Canonical Allele Identifier: CA2270103091

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832467_63832469delinsAAG , CM000679.2:g.63832467_63832469delinsAAG	GRCh38
NC_000017.10:g.61909827_61909829delinsAAG , CM000679.1:g.61909827_61909829delinsAAG	GRCh37
NC_000017.9:g.59263559_59263561delinsAAG	NCBI36
NG_053004.1:g.15523_15525delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2344_2346delinsCTT
ENST00000697953.1:n.2917_2919delinsCTT
ENST00000698013.1:n.3029_3031delinsCTT
ENST00000698014.1:n.3252_3254delinsCTT
ENST00000698015.1:n.2345_2347delinsCTT
ENST00000698016.1:c.*469_*471delinsCTT	ENSP00000513502.1:n.*469_*471delinsCTT
ENST00000698017.1:n.2419_2421delinsCTT
ENST00000698018.1:n.2550_2552delinsCTT
ENST00000698019.1:n.2748_2750delinsCTT
ENST00000698020.1:n.1854_1856delinsCTT
ENST00000698021.1:c.1763_1765delinsCTT
ENST00000698022.1:c.*469_*471delinsCTT	ENSP00000513504.1:n.*469_*471delinsCTT
ENST00000698023.1:n.2448_2450delinsCTT
ENST00000698024.1:n.2310_2312delinsCTT
ENST00000698025.1:n.2470_2472delinsCTT
ENST00000698026.1:n.1361_1363delinsCTT
ENST00000698027.1:c.*686_*688delinsCTT	ENSP00000513505.1:n.*686_*688delinsCTT
ENST00000698028.1:n.2553_2555delinsCTT
ENST00000698029.1:n.3282_3284delinsCTT
ENST00000448276.7:c.*469_*471delinsCTT MANE Select	ENSP00000392617.2:n.*469_*471delinsCTT
ENST00000448276.6:c.*469_*471delinsCTT	ENSP00000392617.2:n.*469_*471delinsCTT
ENST00000613943.4:c.1954_1956delinsCTT	ENSP00000483605.1:n.1954_1956delinsCTT
NM_001098426.1:c.*469_*471delinsCTT	NP_001091896.1:n.*469_*471delinsCTT
XM_005257604.2:c.*469_*471delinsCTT	XP_005257661.2:n.*469_*471delinsCTT
NM_001330439.1:c.*469_*471delinsCTT	NP_001317368.1:n.*469_*471delinsCTT
NM_001330440.1:c.*469_*471delinsCTT	NP_001317369.1:n.*469_*471delinsCTT
NM_001098426.2:c.*469_*471delinsCTT MANE Select	NP_001091896.1:n.*469_*471delinsCTT
NM_001330440.2:c.*469_*471delinsCTT	NP_001317369.1:n.*469_*471delinsCTT