Canonical Allele Identifier: CA2270103418

Gene: SMARCD2

Linked Data

• dbSNP Id: rs2040202849

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832387dup , CM000679.2:g.63832387dup	GRCh38
NC_000017.10:g.61909747dup , CM000679.1:g.61909747dup	GRCh37
NC_000017.9:g.59263479dup	NCBI36
NG_053004.1:g.15605dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2426dup
ENST00000697953.1:n.2999dup
ENST00000698013.1:n.3111dup
ENST00000698014.1:n.3334dup
ENST00000698015.1:n.2427dup
ENST00000698016.1:c.*551dup	ENSP00000513502.1:n.*551dup
ENST00000698017.1:n.2501dup
ENST00000698018.1:n.2632dup
ENST00000698019.1:n.2830dup
ENST00000698020.1:n.1936dup
ENST00000698021.1:c.1845dup
ENST00000698022.1:c.*551dup	ENSP00000513504.1:n.*551dup
ENST00000698023.1:n.2530dup
ENST00000698024.1:n.2392dup
ENST00000698025.1:n.2552dup
ENST00000698026.1:n.1443dup
ENST00000698027.1:c.*768dup	ENSP00000513505.1:n.*768dup
ENST00000698028.1:n.2635dup
ENST00000698029.1:n.3364dup
ENST00000448276.7:c.*551dup MANE Select	ENSP00000392617.2:n.*551dup
ENST00000448276.6:c.*551dup	ENSP00000392617.2:n.*551dup
ENST00000613943.4:c.2036dup	ENSP00000483605.1:n.2036dup
NM_001098426.1:c.*551dup	NP_001091896.1:n.*551dup
XM_005257604.2:c.*551dup	XP_005257661.2:n.*551dup
NM_001330439.1:c.*551dup	NP_001317368.1:n.*551dup
NM_001330440.1:c.*551dup	NP_001317369.1:n.*551dup
NM_001098426.2:c.*551dup MANE Select	NP_001091896.1:n.*551dup
NM_001330440.2:c.*551dup	NP_001317369.1:n.*551dup