Canonical Allele Identifier: CA10303416

Gene: MLC1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50074229del , CM000684.2:g.50074229del	GRCh38
NC_000022.10:g.50512658del , CM000684.1:g.50512658del	GRCh37
NC_000022.9:g.48854785del	NCBI36
NG_009162.1:g.16702del

Transcript Alleles

HGVS	Amino-acid Change
NM_015166.4:c.702del MANE Select	NP_055981.1:p.Trp234Ter
ENST00000311597.10:c.702del MANE Select	ENSP00000310375.6:p.Trp234Ter
NM_001376472.1:c.702del	NP_001363401.1:p.Trp234Ter
NM_001376473.1:c.702del	NP_001363402.1:p.Trp234Ter
NM_001376474.1:c.702del	NP_001363403.1:p.Trp234Ter
NM_001376475.1:c.702del	NP_001363404.1:p.Trp234Ter
NM_001376476.1:c.702del	NP_001363405.1:p.Trp234Ter
NM_001376477.1:c.702del	NP_001363406.1:p.Trp234Ter
NM_001376478.1:c.702del	NP_001363407.1:p.Trp234Ter
NM_001376479.1:c.702del	NP_001363408.1:p.Trp234Ter
NM_001376480.1:c.612del	NP_001363409.1:p.Trp204Ter
NM_001376481.1:c.600del	NP_001363410.1:p.Trp200Ter
NM_001376482.1:c.546del	NP_001363411.1:p.Trp182Ter
NM_001376483.1:c.546del	NP_001363412.1:p.Trp182Ter
NM_001376484.1:c.465del	NP_001363413.1:p.Trp155Ter
NM_015166.3:c.702del	NP_055981.1:p.Trp234Ter
NM_139202.2:c.702del	NP_631941.1:p.Trp234Ter
NM_139202.3:c.702del	NP_631941.1:p.Trp234Ter
NR_164811.1:n.1049del
NR_164812.1:n.833del
NR_164813.1:n.1226del
ENST00000311597.9:c.702del	ENSP00000310375.5:p.Trp234Ter
ENST00000395876.6:c.702del	ENSP00000379216.2:p.Trp234Ter
ENST00000442311.1:c.612del	ENSP00000401385.1:p.Trp204Ter
ENST00000470008.1:n.182del
XM_011530678.1:c.702del	XP_011528980.1:p.Trp234Ter
XM_011530678.2:c.702del	XP_011528980.1:p.Trp234Ter
XM_017028671.1:c.702del	XP_016884160.1:p.Trp234Ter
XR_001755180.2:n.1207del
XR_001755181.2:n.975del
XR_430476.2:n.1097del