Canonical Allele Identifier: CA2693805852
Gene: SMC1A HGNC NCBI

Linked Data

gnomAD v4: X-53414683-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53414683G>T , CM000685.2:g.53414683G>T GRCh38
NC_000023.10:g.53441632G>T , CM000685.1:g.53441632G>T GRCh37
NC_000023.9:g.53458357G>T NCBI36
NG_006988.2:g.12988C>A , LRG_773:g.12988C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000322213.9:c.411+75C>A MANE Select ENSP00000323421.3:n.411+75C>A
ENST00000674590.1:c.345+75C>A ENSP00000502626.1:n.345+75C>A
ENST00000675065.1:n.465+75C>A
ENST00000675504.1:c.345+75C>A ENSP00000502524.1:n.345+75C>A
ENST00000322213.8:c.411+75C>A ENSP00000323421.3:n.411+75C>A
ENST00000375340.10:c.345+75C>A ENSP00000364489.7:n.345+75C>A
ENST00000428014.1:c.345+75C>A ENSP00000413509.2:n.345+75C>A
ENST00000463684.1:c.110-1248C>A ENSP00000476958.1:n.110-1248C>A
NM_001281463.1:c.345+75C>A , LRG_773t1:c.345+75C>A NP_001268392.1:n.345+75C>A
NM_006306.3:c.411+75C>A , LRG_773t2:c.411+75C>A NP_006297.2:n.411+75C>A
NM_006306.4:c.411+75C>A MANE Select NP_006297.2:n.411+75C>A