Canonical Allele Identifier: CA16042030
Gene: MLC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 370785
dbSNP Id: rs1057516766

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50084767del , CM000684.2:g.50084767del GRCh38
NC_000022.10:g.50523196del , CM000684.1:g.50523196del GRCh37
NC_000022.9:g.48865323del NCBI36
NG_009162.1:g.6163del

Transcript Alleles

HGVS Amino-acid change
ENST00000311597.10:c.136del MANE Select ENSP00000310375.6:p.Cys46AlafsTer12
ENST00000311597.9:c.136del ENSP00000310375.5:p.Cys46AlafsTer12
ENST00000395876.6:c.136del ENSP00000379216.2:p.Cys46AlafsTer12
ENST00000442311.1:c.136del ENSP00000401385.1:p.Cys46AlafsTer12
NM_015166.3:c.136del NP_055981.1:p.Cys46AlafsTer12
NM_139202.2:c.136del NP_631941.1:p.Cys46AlafsTer12
XM_011530678.1:c.136del XP_011528980.1:p.Cys46AlafsTer12
XR_430476.2:n.531del
XM_011530678.2:c.136del XP_011528980.1:p.Cys46AlafsTer12
XM_017028671.1:c.136del XP_016884160.1:p.Cys46AlafsTer12
XR_001755180.2:n.641del
XR_001755181.2:n.409del
NM_001376472.1:c.136del NP_001363401.1:p.Cys46AlafsTer12
NM_001376473.1:c.136del NP_001363402.1:p.Cys46AlafsTer12
NM_001376474.1:c.136del NP_001363403.1:p.Cys46AlafsTer12
NM_001376475.1:c.136del NP_001363404.1:p.Cys46AlafsTer12
NM_001376476.1:c.136del NP_001363405.1:p.Cys46AlafsTer12
NM_001376477.1:c.136del NP_001363406.1:p.Cys46AlafsTer12
NM_001376478.1:c.136del NP_001363407.1:p.Cys46AlafsTer12
NM_001376479.1:c.136del NP_001363408.1:p.Cys46AlafsTer12
NM_001376480.1:c.136del NP_001363409.1:p.Cys46AlafsTer12
NM_001376481.1:c.136del NP_001363410.1:p.Cys46AlafsTer12
NM_001376482.1:c.136del NP_001363411.1:p.Cys46AlafsTer12
NM_001376483.1:c.136del NP_001363412.1:p.Cys46AlafsTer12
NM_001376484.1:c.-59+588del NP_001363413.1:n.-59+588del
NM_015166.4:c.136del MANE Select NP_055981.1:p.Cys46AlafsTer12
NM_139202.3:c.136del NP_631941.1:p.Cys46AlafsTer12
NR_164811.1:n.483del
NR_164812.1:n.267del
NR_164813.1:n.660del