Canonical Allele Identifier: CA412110630

Gene: MLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50079948G>T , CM000684.2:g.50079948G>T	GRCh38
NC_000022.10:g.50518377G>T , CM000684.1:g.50518377G>T	GRCh37
NC_000022.9:g.48860504G>T	NCBI36
NG_009162.1:g.10982C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015166.4:c.393C>A MANE Select	NP_055981.1:p.Cys131Ter
ENST00000311597.10:c.393C>A MANE Select	ENSP00000310375.6:p.Cys131Ter
NM_001376472.1:c.393C>A	NP_001363401.1:p.Cys131Ter
NM_001376473.1:c.393C>A	NP_001363402.1:p.Cys131Ter
NM_001376474.1:c.393C>A	NP_001363403.1:p.Cys131Ter
NM_001376475.1:c.393C>A	NP_001363404.1:p.Cys131Ter
NM_001376476.1:c.393C>A	NP_001363405.1:p.Cys131Ter
NM_001376477.1:c.393C>A	NP_001363406.1:p.Cys131Ter
NM_001376478.1:c.393C>A	NP_001363407.1:p.Cys131Ter
NM_001376479.1:c.393C>A	NP_001363408.1:p.Cys131Ter
NM_001376480.1:c.303C>A	NP_001363409.1:p.Cys101Ter
NM_001376481.1:c.321+396C>A	NP_001363410.1:n.321+396C>A
NM_001376482.1:c.268-2446C>A	NP_001363411.1:n.268-2446C>A
NM_001376483.1:c.268-2446C>A	NP_001363412.1:n.268-2446C>A
NM_001376484.1:c.156C>A	NP_001363413.1:p.Cys52Ter
NM_015166.3:c.393C>A	NP_055981.1:p.Cys131Ter
NM_139202.2:c.393C>A	NP_631941.1:p.Cys131Ter
NM_139202.3:c.393C>A	NP_631941.1:p.Cys131Ter
NR_164811.1:n.740C>A
NR_164812.1:n.524C>A
NR_164813.1:n.917C>A
ENST00000311597.9:c.393C>A	ENSP00000310375.5:p.Cys131Ter
ENST00000395876.6:c.393C>A	ENSP00000379216.2:p.Cys131Ter
ENST00000442311.1:c.303C>A	ENSP00000401385.1:p.Cys101Ter
XM_011530678.1:c.393C>A	XP_011528980.1:p.Cys131Ter
XM_011530678.2:c.393C>A	XP_011528980.1:p.Cys131Ter
XM_017028671.1:c.393C>A	XP_016884160.1:p.Cys131Ter
XR_001755180.2:n.898C>A
XR_001755181.2:n.666C>A
XR_430476.2:n.788C>A