Canonical Allele Identifier: CA413243369

Gene: SMC1A

Linked Data

• MyVariant Identifiers: chrX:g.53409217T>G (hg19) ; chrX:g.53382296T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53382296T>G , CM000685.2:g.53382296T>G	GRCh38
NC_000023.10:g.53409217T>G , CM000685.1:g.53409217T>G	GRCh37
NC_000023.9:g.53425942T>G	NCBI36
NG_006988.2:g.45375A>C , LRG_773:g.45375A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000322213.9:c.3373A>C MANE Select	ENSP00000323421.3:p.Met1125Leu
ENST00000674590.1:c.2605A>C	ENSP00000502626.1:p.Met869Leu
ENST00000675504.1:c.3307A>C	ENSP00000502524.1:p.Met1103Leu
ENST00000322213.8:c.3373A>C	ENSP00000323421.3:p.Met1125Leu
ENST00000375340.10:c.3307A>C	ENSP00000364489.7:p.Met1103Leu
ENST00000469129.1:n.229A>C
ENST00000470241.2:c.663A>C
NM_001281463.1:c.3307A>C , LRG_773t1:c.3307A>C	NP_001268392.1:p.Met1103Leu
NM_006306.3:c.3373A>C , LRG_773t2:c.3373A>C	NP_006297.2:p.Met1125Leu
NM_006306.4:c.3373A>C MANE Select	NP_006297.2:p.Met1125Leu