Canonical Allele Identifier: CA2693803801

Gene: SMC1A

Linked Data

• gnomAD v4: X-53382173-GAGCCTCTGGTGGCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53382174_53382188del , CM000685.2:g.53382174_53382188del	GRCh38
NC_000023.10:g.53409095_53409109del , CM000685.1:g.53409095_53409109del	GRCh37
NC_000023.9:g.53425820_53425834del	NCBI36
NG_006988.2:g.45483_45497del , LRG_773:g.45483_45497del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322213.9:c.3437+44_3437+58del MANE Select	ENSP00000323421.3:n.3437+44_3437+58del
ENST00000674590.1:c.2669+44_2669+58del	ENSP00000502626.1:n.2669+44_2669+58del
ENST00000675504.1:c.3371+44_3371+58del	ENSP00000502524.1:n.3371+44_3371+58del
ENST00000322213.8:c.3437+44_3437+58del	ENSP00000323421.3:n.3437+44_3437+58del
ENST00000375340.10:c.3371+44_3371+58del	ENSP00000364489.7:n.3371+44_3371+58del
ENST00000469129.1:n.337_351del
ENST00000470241.2:c.727+44_727+58del
NM_001281463.1:c.3371+44_3371+58del , LRG_773t1:c.3371+44_3371+58del	NP_001268392.1:n.3371+44_3371+58del
NM_006306.3:c.3437+44_3437+58del , LRG_773t2:c.3437+44_3437+58del	NP_006297.2:n.3437+44_3437+58del
NM_006306.4:c.3437+44_3437+58del MANE Select	NP_006297.2:n.3437+44_3437+58del