Canonical Allele Identifier: CA2270103360

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832331_63832332delinsCA , CM000679.2:g.63832331_63832332delinsCA	GRCh38
NC_000017.10:g.61909691_61909692delinsCA , CM000679.1:g.61909691_61909692delinsCA	GRCh37
NC_000017.9:g.59263423_59263424delinsCA	NCBI36
NG_053004.1:g.15660_15661delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2481_2482delinsTG
ENST00000697953.1:n.3054_3055delinsTG
ENST00000698013.1:n.3166_3167delinsTG
ENST00000698014.1:n.3389_3390delinsTG
ENST00000698015.1:n.2482_2483delinsTG
ENST00000698016.1:c.*606_*607delinsTG	ENSP00000513502.1:n.*606_*607delinsTG
ENST00000698017.1:n.2556_2557delinsTG
ENST00000698018.1:n.2687_2688delinsTG
ENST00000698019.1:n.2885_2886delinsTG
ENST00000698020.1:n.1991_1992delinsTG
ENST00000698021.1:c.1900_1901delinsTG
ENST00000698022.1:c.*606_*607delinsTG	ENSP00000513504.1:n.*606_*607delinsTG
ENST00000698023.1:n.2585_2586delinsTG
ENST00000698024.1:n.2447_2448delinsTG
ENST00000698025.1:n.2607_2608delinsTG
ENST00000698026.1:n.1498_1499delinsTG
ENST00000698027.1:c.*823_*824delinsTG	ENSP00000513505.1:n.*823_*824delinsTG
ENST00000698028.1:n.2690_2691delinsTG
ENST00000698029.1:n.3419_3420delinsTG
ENST00000448276.7:c.*606_*607delinsTG MANE Select	ENSP00000392617.2:n.*606_*607delinsTG
ENST00000448276.6:c.*606_*607delinsTG	ENSP00000392617.2:n.*606_*607delinsTG
ENST00000613943.4:c.2091_2092delinsTG	ENSP00000483605.1:n.2091_2092delinsTG
NM_001098426.1:c.*606_*607delinsTG	NP_001091896.1:n.*606_*607delinsTG
XM_005257604.2:c.*606_*607delinsTG	XP_005257661.2:n.*606_*607delinsTG
NM_001330439.1:c.*606_*607delinsTG	NP_001317368.1:n.*606_*607delinsTG
NM_001330440.1:c.*606_*607delinsTG	NP_001317369.1:n.*606_*607delinsTG
NM_001098426.2:c.*606_*607delinsTG MANE Select	NP_001091896.1:n.*606_*607delinsTG
NM_001330440.2:c.*606_*607delinsTG	NP_001317369.1:n.*606_*607delinsTG