Canonical Allele Identifier: CA2270103128

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832557_63832558delinsCT , CM000679.2:g.63832557_63832558delinsCT	GRCh38
NC_000017.10:g.61909917_61909918delinsCT , CM000679.1:g.61909917_61909918delinsCT	GRCh37
NC_000017.9:g.59263649_59263650delinsCT	NCBI36
NG_053004.1:g.15434_15435delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2255_2256delinsAG
ENST00000697953.1:n.2828_2829delinsAG
ENST00000698013.1:n.2940_2941delinsAG
ENST00000698014.1:n.3163_3164delinsAG
ENST00000698015.1:n.2256_2257delinsAG
ENST00000698016.1:c.*380_*381delinsAG	ENSP00000513502.1:n.*380_*381delinsAG
ENST00000698017.1:n.2330_2331delinsAG
ENST00000698018.1:n.2461_2462delinsAG
ENST00000698019.1:n.2659_2660delinsAG
ENST00000698020.1:n.1765_1766delinsAG
ENST00000698021.1:c.1674_1675delinsAG
ENST00000698022.1:c.*380_*381delinsAG	ENSP00000513504.1:n.*380_*381delinsAG
ENST00000698023.1:n.2359_2360delinsAG
ENST00000698024.1:n.2221_2222delinsAG
ENST00000698025.1:n.2381_2382delinsAG
ENST00000698026.1:n.1272_1273delinsAG
ENST00000698027.1:c.*597_*598delinsAG	ENSP00000513505.1:n.*597_*598delinsAG
ENST00000698028.1:n.2464_2465delinsAG
ENST00000698029.1:n.3193_3194delinsAG
ENST00000448276.7:c.*380_*381delinsAG MANE Select	ENSP00000392617.2:n.*380_*381delinsAG
ENST00000323347.14:c.*380_*381delinsAG	ENSP00000318451.10:n.*380_*381delinsAG
ENST00000448276.6:c.*380_*381delinsAG	ENSP00000392617.2:n.*380_*381delinsAG
ENST00000613943.4:c.1865_1866delinsAG	ENSP00000483605.1:n.1865_1866delinsAG
NM_001098426.1:c.*380_*381delinsAG	NP_001091896.1:n.*380_*381delinsAG
XM_005257604.2:c.*380_*381delinsAG	XP_005257661.2:n.*380_*381delinsAG
NM_001330439.1:c.*380_*381delinsAG	NP_001317368.1:n.*380_*381delinsAG
NM_001330440.1:c.*380_*381delinsAG	NP_001317369.1:n.*380_*381delinsAG
NM_001098426.2:c.*380_*381delinsAG MANE Select	NP_001091896.1:n.*380_*381delinsAG
NM_001330440.2:c.*380_*381delinsAG	NP_001317369.1:n.*380_*381delinsAG