Canonical Allele Identifier: CA412111551
Community Standard Title: NM_015166.4(MLC1):c.254G>A (p.Cys85Tyr)
Gene: MLC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50083097C>T , CM000684.2:g.50083097C>T GRCh38
NC_000022.10:g.50521526C>T , CM000684.1:g.50521526C>T GRCh37
NC_000022.9:g.48863653C>T NCBI36
NG_009162.1:g.7833G>A

Transcript Alleles

HGVS Amino-acid Change
NM_015166.4:c.254G>A MANE Select NP_055981.1:p.Cys85Tyr
ENST00000311597.10:c.254G>A MANE Select ENSP00000310375.6:p.Cys85Tyr
NM_001376472.1:c.254G>A NP_001363401.1:p.Cys85Tyr
NM_001376473.1:c.254G>A NP_001363402.1:p.Cys85Tyr
NM_001376474.1:c.254G>A NP_001363403.1:p.Cys85Tyr
NM_001376475.1:c.254G>A NP_001363404.1:p.Cys85Tyr
NM_001376476.1:c.254G>A NP_001363405.1:p.Cys85Tyr
NM_001376477.1:c.254G>A NP_001363406.1:p.Cys85Tyr
NM_001376478.1:c.254G>A NP_001363407.1:p.Cys85Tyr
NM_001376479.1:c.254G>A NP_001363408.1:p.Cys85Tyr
NM_001376480.1:c.177+1629G>A NP_001363409.1:n.177+1629G>A
NM_001376481.1:c.254G>A NP_001363410.1:p.Cys85Tyr
NM_001376482.1:c.254G>A NP_001363411.1:p.Cys85Tyr
NM_001376483.1:c.254G>A NP_001363412.1:p.Cys85Tyr
NM_001376484.1:c.17G>A NP_001363413.1:p.Cys6Tyr
NM_015166.3:c.254G>A NP_055981.1:p.Cys85Tyr
NM_139202.2:c.254G>A NP_631941.1:p.Cys85Tyr
NM_139202.3:c.254G>A NP_631941.1:p.Cys85Tyr
NR_164811.1:n.601G>A
NR_164812.1:n.385G>A
NR_164813.1:n.778G>A
ENST00000311597.9:c.254G>A ENSP00000310375.5:p.Cys85Tyr
ENST00000395876.6:c.254G>A ENSP00000379216.2:p.Cys85Tyr
ENST00000442311.1:c.177+1629G>A ENSP00000401385.1:n.177+1629G>A
XM_011530678.1:c.254G>A XP_011528980.1:p.Cys85Tyr
XM_011530678.2:c.254G>A XP_011528980.1:p.Cys85Tyr
XM_017028671.1:c.254G>A XP_016884160.1:p.Cys85Tyr
XR_001755180.2:n.759G>A
XR_001755181.2:n.527G>A
XR_430476.2:n.649G>A