Canonical Allele Identifier: CA412110528
Gene: MLC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50079918G>C , CM000684.2:g.50079918G>C GRCh38
NC_000022.10:g.50518347G>C , CM000684.1:g.50518347G>C GRCh37
NC_000022.9:g.48860474G>C NCBI36
NG_009162.1:g.11012C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311597.10:c.423C>G MANE Select ENSP00000310375.6:p.Asn141Lys
ENST00000311597.9:c.423C>G ENSP00000310375.5:p.Asn141Lys
ENST00000395876.6:c.423C>G ENSP00000379216.2:p.Asn141Lys
ENST00000442311.1:c.333C>G ENSP00000401385.1:p.Asn111Lys
NM_015166.3:c.423C>G NP_055981.1:p.Asn141Lys
NM_139202.2:c.423C>G NP_631941.1:p.Asn141Lys
XM_011530678.1:c.423C>G XP_011528980.1:p.Asn141Lys
XR_430476.2:n.818C>G
XM_011530678.2:c.423C>G XP_011528980.1:p.Asn141Lys
XM_017028671.1:c.423C>G XP_016884160.1:p.Asn141Lys
XR_001755180.2:n.928C>G
XR_001755181.2:n.696C>G
NM_001376472.1:c.423C>G NP_001363401.1:p.Asn141Lys
NM_001376473.1:c.423C>G NP_001363402.1:p.Asn141Lys
NM_001376474.1:c.423C>G NP_001363403.1:p.Asn141Lys
NM_001376475.1:c.423C>G NP_001363404.1:p.Asn141Lys
NM_001376476.1:c.423C>G NP_001363405.1:p.Asn141Lys
NM_001376477.1:c.423C>G NP_001363406.1:p.Asn141Lys
NM_001376478.1:c.423C>G NP_001363407.1:p.Asn141Lys
NM_001376479.1:c.423C>G NP_001363408.1:p.Asn141Lys
NM_001376480.1:c.333C>G NP_001363409.1:p.Asn111Lys
NM_001376481.1:c.321+426C>G NP_001363410.1:n.321+426C>G
NM_001376482.1:c.268-2416C>G NP_001363411.1:n.268-2416C>G
NM_001376483.1:c.268-2416C>G NP_001363412.1:n.268-2416C>G
NM_001376484.1:c.186C>G NP_001363413.1:p.Asn62Lys
NM_015166.4:c.423C>G MANE Select NP_055981.1:p.Asn141Lys
NM_139202.3:c.423C>G NP_631941.1:p.Asn141Lys
NR_164811.1:n.770C>G
NR_164812.1:n.554C>G
NR_164813.1:n.947C>G