Canonical Allele Identifier: CA2270105625

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837644_63837645delinsCG , CM000679.2:g.63837644_63837645delinsCG	GRCh38
NC_000017.10:g.61915004_61915005delinsCG , CM000679.1:g.61915004_61915005delinsCG	GRCh37
NC_000017.9:g.59268736_59268737delinsCG	NCBI36
NG_053004.1:g.10347_10348delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.105-20_105-19delinsCG
ENST00000698016.1:c.56_57delinsCG	ENSP00000513502.1:p.Pro19=
ENST00000698022.1:c.34-20_34-19delinsCG	ENSP00000513504.1:n.34-20_34-19delinsCG
ENST00000698027.1:c.56_57delinsCG	ENSP00000513505.1:p.Pro19=
ENST00000448276.7:c.217-20_217-19delinsCG MANE Select	ENSP00000392617.2:n.217-20_217-19delinsCG
ENST00000225742.13:c.-9-20_-9-19delinsCG	ENSP00000225742.9:n.-9-20_-9-19delinsCG
ENST00000323347.14:c.73-20_73-19delinsCG	ENSP00000318451.10:n.73-20_73-19delinsCG
ENST00000448276.6:c.217-20_217-19delinsCG	ENSP00000392617.2:n.217-20_217-19delinsCG
ENST00000577686.1:n.53-408_53-407delinsCG
ENST00000584400.5:c.217-408_217-407delinsCG	ENSP00000464503.1:n.217-408_217-407delinsCG
ENST00000613943.4:c.106-20_106-19delinsCG	ENSP00000483605.1:n.106-20_106-19delinsCG
NM_001098426.1:c.217-20_217-19delinsCG	NP_001091896.1:n.217-20_217-19delinsCG
XM_005257604.2:c.-9-20_-9-19delinsCG	XP_005257661.2:n.-9-20_-9-19delinsCG
NM_001330439.1:c.-9-20_-9-19delinsCG	NP_001317368.1:n.-9-20_-9-19delinsCG
NM_001330440.1:c.73-20_73-19delinsCG	NP_001317369.1:n.73-20_73-19delinsCG
NM_001098426.2:c.217-20_217-19delinsCG MANE Select	NP_001091896.1:n.217-20_217-19delinsCG
NM_001330440.2:c.73-20_73-19delinsCG	NP_001317369.1:n.73-20_73-19delinsCG