Canonical Allele Identifier: CA516688854
Gene: SMC1A HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.53440080C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53413130C>T , CM000685.2:g.53413130C>T GRCh38
NC_000023.10:g.53440080C>T , CM000685.1:g.53440080C>T GRCh37
NC_000023.9:g.53456805C>T NCBI36
NG_006988.2:g.14541G>A , LRG_773:g.14541G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000322213.9:c.624G>A MANE Select ENSP00000323421.3:p.Arg208=
ENST00000674590.1:c.346-1229G>A ENSP00000502626.1:n.346-1229G>A
ENST00000675065.1:n.466-1229G>A
ENST00000675504.1:c.558G>A ENSP00000502524.1:p.Arg186=
ENST00000322213.8:c.624G>A ENSP00000323421.3:p.Arg208=
ENST00000375340.10:c.558G>A ENSP00000364489.7:p.Arg186=
ENST00000428014.1:c.558G>A ENSP00000413509.2:p.Arg186=
ENST00000463684.1:c.*157G>A ENSP00000476958.1:n.*157G>A
NM_001281463.1:c.558G>A , LRG_773t1:c.558G>A NP_001268392.1:p.Arg186=
NM_006306.3:c.624G>A , LRG_773t2:c.624G>A NP_006297.2:p.Arg208=
NM_006306.4:c.624G>A MANE Select NP_006297.2:p.Arg208=