Canonical Allele Identifier: CA516553641
Gene: SMC1A HGNC NCBI

Linked Data

dbSNP Id: rs782763816
MyVariant Identifiers: chrX:g.53407625C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53380704C>A , CM000685.2:g.53380704C>A GRCh38
NC_000023.10:g.53407625C>A , CM000685.1:g.53407625C>A GRCh37
NC_000023.9:g.53424350C>A NCBI36
NG_006988.2:g.46967G>T , LRG_773:g.46967G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.3534G>T MANE Select ENSP00000323421.3:p.Ser1178=
ENST00000674590.1:c.2766G>T ENSP00000502626.1:p.Ser922=
ENST00000675504.1:c.3468G>T ENSP00000502524.1:p.Ser1156=
ENST00000322213.8:c.3534G>T ENSP00000323421.3:p.Ser1178=
ENST00000375340.10:c.3468G>T ENSP00000364489.7:p.Ser1156=
ENST00000470241.2:c.754G>T
NM_001281463.1:c.3468G>T , LRG_773t1:c.3468G>T NP_001268392.1:p.Ser1156=
NM_006306.3:c.3534G>T , LRG_773t2:c.3534G>T NP_006297.2:p.Ser1178=
NM_006306.4:c.3534G>T MANE Select NP_006297.2:p.Ser1178=