Canonical Allele Identifier: CA516561949
Community Standard Title: NM_006306.4(SMC1A):c.1404G>A (p.Arg468=)
Gene: SMC1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53409203C>T , CM000685.2:g.53409203C>T GRCh38
NC_000023.10:g.53436134C>T , CM000685.1:g.53436134C>T GRCh37
NC_000023.9:g.53452859C>T NCBI36
NG_006988.2:g.18468G>A , LRG_773:g.18468G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006306.4:c.1404G>A MANE Select NP_006297.2:p.Arg468=
ENST00000322213.9:c.1404G>A MANE Select ENSP00000323421.3:p.Arg468=
NM_001281463.1:c.1338G>A , LRG_773t1:c.1338G>A NP_001268392.1:p.Arg446=
NM_006306.3:c.1404G>A , LRG_773t2:c.1404G>A NP_006297.2:p.Arg468=
ENST00000322213.8:c.1404G>A ENSP00000323421.3:p.Arg468=
ENST00000375340.10:c.1338G>A ENSP00000364489.7:p.Arg446=
ENST00000674590.1:c.636G>A ENSP00000502626.1:p.Arg212=
ENST00000675065.1:n.756G>A
ENST00000675504.1:c.1338G>A ENSP00000502524.1:p.Arg446=