Canonical Allele Identifier: CA413252547

Gene: SMC1A

Linked Data

• MyVariant Identifiers: chrX:g.53432298A>G (hg19) ; chrX:g.53405366A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53405366A>G , CM000685.2:g.53405366A>G	GRCh38
NC_000023.10:g.53432298A>G , CM000685.1:g.53432298A>G	GRCh37
NC_000023.9:g.53449023A>G	NCBI36
NG_006988.2:g.22305T>C , LRG_773:g.22305T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.1937T>C MANE Select	ENSP00000323421.3:p.Phe646Ser
ENST00000674590.1:c.1169T>C	ENSP00000502626.1:p.Phe390Ser
ENST00000675065.1:n.1289T>C
ENST00000675504.1:c.1871T>C	ENSP00000502524.1:p.Phe624Ser
ENST00000322213.8:c.1937T>C	ENSP00000323421.3:p.Phe646Ser
ENST00000375340.10:c.1871T>C	ENSP00000364489.7:p.Phe624Ser
NM_001281463.1:c.1871T>C , LRG_773t1:c.1871T>C	NP_001268392.1:p.Phe624Ser
NM_006306.3:c.1937T>C , LRG_773t2:c.1937T>C	NP_006297.2:p.Phe646Ser
NM_006306.4:c.1937T>C MANE Select	NP_006297.2:p.Phe646Ser