Canonical Allele Identifier: CA384792124
Community Standard Title: NM_003076.5(SMARCD1):c.990C>G (p.Asp330Glu)
Gene: SMARCD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.50090357C>G , CM000674.2:g.50090357C>G GRCh38
NC_000012.11:g.50484140C>G , CM000674.1:g.50484140C>G GRCh37
NC_000012.10:g.48770407C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_003076.5:c.990C>G MANE Select NP_003067.3:p.Asp330Glu
ENST00000394963.9:c.990C>G MANE Select ENSP00000378414.4:p.Asp330Glu
NM_003076.4:c.990C>G NP_003067.3:p.Asp330Glu
NM_139071.2:c.990C>G NP_620710.2:p.Asp330Glu
NM_139071.3:c.990C>G NP_620710.2:p.Asp330Glu
ENST00000381513.8:c.990C>G ENSP00000370924.4:p.Asp330Glu
ENST00000394963.8:c.990C>G ENSP00000378414.4:p.Asp330Glu
ENST00000548573.5:c.384C>G ENSP00000448627.1:p.Asp128Glu
ENST00000550477.5:c.750C>G ENSP00000448030.1:p.Asp250Glu
XM_005269107.3:c.867C>G XP_005269164.2:p.Asp289Glu
XM_005269107.4:c.867C>G XP_005269164.2:p.Asp289Glu
XR_944683.1:n.1160C>G
XR_944683.2:n.1124C>G
XR_944684.1:n.1160C>G
XR_944684.2:n.1124C>G