Canonical Allele Identifier: CA2810124108

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832364A>T , CM000679.2:g.63832364A>T	GRCh38
NC_000017.10:g.61909724A>T , CM000679.1:g.61909724A>T	GRCh37
NC_000017.9:g.59263456A>T	NCBI36
NG_053004.1:g.15628T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2449T>A
ENST00000697953.1:n.3022T>A
ENST00000698013.1:n.3134T>A
ENST00000698014.1:n.3357T>A
ENST00000698015.1:n.2450T>A
ENST00000698016.1:c.*574T>A	ENSP00000513502.1:n.*574T>A
ENST00000698017.1:n.2524T>A
ENST00000698018.1:n.2655T>A
ENST00000698019.1:n.2853T>A
ENST00000698020.1:n.1959T>A
ENST00000698021.1:c.1868T>A
ENST00000698022.1:c.*574T>A	ENSP00000513504.1:n.*574T>A
ENST00000698023.1:n.2553T>A
ENST00000698024.1:n.2415T>A
ENST00000698025.1:n.2575T>A
ENST00000698026.1:n.1466T>A
ENST00000698027.1:c.*791T>A	ENSP00000513505.1:n.*791T>A
ENST00000698028.1:n.2658T>A
ENST00000698029.1:n.3387T>A
ENST00000448276.7:c.*574T>A MANE Select	ENSP00000392617.2:n.*574T>A
ENST00000448276.6:c.*574T>A	ENSP00000392617.2:n.*574T>A
ENST00000613943.4:c.2059T>A	ENSP00000483605.1:n.2059T>A
NM_001098426.1:c.*574T>A	NP_001091896.1:n.*574T>A
XM_005257604.2:c.*574T>A	XP_005257661.2:n.*574T>A
NM_001330439.1:c.*574T>A	NP_001317368.1:n.*574T>A
NM_001330440.1:c.*574T>A	NP_001317369.1:n.*574T>A
NM_001098426.2:c.*574T>A MANE Select	NP_001091896.1:n.*574T>A
NM_001330440.2:c.*574T>A	NP_001317369.1:n.*574T>A