Canonical Allele Identifier: CA641906917

Gene: SMC1A

Linked Data

• ClinVar Variation Id: 1548931
• ClinVar RCV Id: RCV002187152
• dbSNP Id: rs1556890636
• gnomAD v2: X-53439216-G-A
• gnomAD v4: X-53412266-G-A
• MyVariant Identifiers: chrX:g.53439216G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53412266G>A , CM000685.2:g.53412266G>A	GRCh38
NC_000023.10:g.53439216G>A , CM000685.1:g.53439216G>A	GRCh37
NC_000023.9:g.53455941G>A	NCBI36
NG_006988.2:g.15405C>T , LRG_773:g.15405C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000322213.9:c.855-13C>T MANE Select	ENSP00000323421.3:n.855-13C>T
ENST00000674590.1:c.346-365C>T	ENSP00000502626.1:n.346-365C>T
ENST00000675065.1:n.466-365C>T
ENST00000675504.1:c.789-13C>T	ENSP00000502524.1:n.789-13C>T
ENST00000322213.8:c.855-13C>T	ENSP00000323421.3:n.855-13C>T
ENST00000375340.10:c.789-13C>T	ENSP00000364489.7:n.789-13C>T
ENST00000463684.1:c.*388-13C>T	ENSP00000476958.1:n.*388-13C>T
NM_001281463.1:c.789-13C>T , LRG_773t1:c.789-13C>T	NP_001268392.1:n.789-13C>T
NM_006306.3:c.855-13C>T , LRG_773t2:c.855-13C>T	NP_006297.2:n.855-13C>T
NM_006306.4:c.855-13C>T MANE Select	NP_006297.2:n.855-13C>T