Canonical Allele Identifier: CA2429817392
Gene: SMC1A HGNC NCBI

Linked Data

dbSNP Id: rs2075585842
gnomAD v4: X-53382191-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53382191G>A , CM000685.2:g.53382191G>A GRCh38
NC_000023.10:g.53409112G>A , CM000685.1:g.53409112G>A GRCh37
NC_000023.9:g.53425837G>A NCBI36
NG_006988.2:g.45480C>T , LRG_773:g.45480C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.3437+41C>T MANE Select ENSP00000323421.3:n.3437+41C>T
ENST00000674590.1:c.2669+41C>T ENSP00000502626.1:n.2669+41C>T
ENST00000675504.1:c.3371+41C>T ENSP00000502524.1:n.3371+41C>T
ENST00000322213.8:c.3437+41C>T ENSP00000323421.3:n.3437+41C>T
ENST00000375340.10:c.3371+41C>T ENSP00000364489.7:n.3371+41C>T
ENST00000469129.1:n.334C>T
ENST00000470241.2:c.727+41C>T
NM_001281463.1:c.3371+41C>T , LRG_773t1:c.3371+41C>T NP_001268392.1:n.3371+41C>T
NM_006306.3:c.3437+41C>T , LRG_773t2:c.3437+41C>T NP_006297.2:n.3437+41C>T
NM_006306.4:c.3437+41C>T MANE Select NP_006297.2:n.3437+41C>T