Canonical Allele Identifier: CA2693805257
Gene: SMC1A HGNC NCBI
MIR6857 HGNC NCBI

Linked Data

gnomAD v4: X-53405725-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53405725A>C , CM000685.2:g.53405725A>C GRCh38
NC_000023.10:g.53432657A>C , CM000685.1:g.53432657A>C GRCh37
NC_000023.9:g.53449382A>C NCBI36
NG_006988.2:g.21946T>G , LRG_773:g.21946T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000322213.9:c.1731+46T>G (SMC1A) MANE Select ENSP00000323421.3:n.1731+46T>G
ENST00000674590.1:c.963+46T>G (SMC1A) ENSP00000502626.1:n.963+46T>G
ENST00000675065.1:n.1083+46T>G (SMC1A)
ENST00000675504.1:c.1665+46T>G (SMC1A) ENSP00000502524.1:n.1665+46T>G
ENST00000322213.8:c.1731+46T>G (SMC1A) ENSP00000323421.3:n.1731+46T>G
ENST00000375340.10:c.1665+46T>G (SMC1A) ENSP00000364489.7:n.1665+46T>G
NM_001281463.1:c.1665+46T>G , LRG_773t1:c.1665+46T>G (SMC1A) NP_001268392.1:n.1665+46T>G
NM_006306.3:c.1731+46T>G , LRG_773t2:c.1731+46T>G (SMC1A) NP_006297.2:n.1731+46T>G
NR_106916.1:n.41T>G (MIR6857)
NM_006306.4:c.1731+46T>G (SMC1A) MANE Select NP_006297.2:n.1731+46T>G