Canonical Allele Identifier: CA412109330

Gene: MLC1

Linked Data

• COSMIC: COSM4926781
• MyVariant Identifiers: chr22:g.50512719T>C (hg19) ; chr22:g.50074290T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50074290T>C , CM000684.2:g.50074290T>C	GRCh38
NC_000022.10:g.50512719T>C , CM000684.1:g.50512719T>C	GRCh37
NC_000022.9:g.48854846T>C	NCBI36
NG_009162.1:g.16640A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311597.10:c.640A>G MANE Select	ENSP00000310375.6:p.Ile214Val
ENST00000311597.9:c.640A>G	ENSP00000310375.5:p.Ile214Val
ENST00000395876.6:c.640A>G	ENSP00000379216.2:p.Ile214Val
ENST00000442311.1:c.550A>G	ENSP00000401385.1:p.Ile184Val
ENST00000470008.1:n.120A>G
NM_015166.3:c.640A>G	NP_055981.1:p.Ile214Val
NM_139202.2:c.640A>G	NP_631941.1:p.Ile214Val
XM_011530678.1:c.640A>G	XP_011528980.1:p.Ile214Val
XR_430476.2:n.1035A>G
XM_011530678.2:c.640A>G	XP_011528980.1:p.Ile214Val
XM_017028671.1:c.640A>G	XP_016884160.1:p.Ile214Val
XR_001755180.2:n.1145A>G
XR_001755181.2:n.913A>G
NM_001376472.1:c.640A>G	NP_001363401.1:p.Ile214Val
NM_001376473.1:c.640A>G	NP_001363402.1:p.Ile214Val
NM_001376474.1:c.640A>G	NP_001363403.1:p.Ile214Val
NM_001376475.1:c.640A>G	NP_001363404.1:p.Ile214Val
NM_001376476.1:c.640A>G	NP_001363405.1:p.Ile214Val
NM_001376477.1:c.640A>G	NP_001363406.1:p.Ile214Val
NM_001376478.1:c.640A>G	NP_001363407.1:p.Ile214Val
NM_001376479.1:c.640A>G	NP_001363408.1:p.Ile214Val
NM_001376480.1:c.550A>G	NP_001363409.1:p.Ile184Val
NM_001376481.1:c.538A>G	NP_001363410.1:p.Ile180Val
NM_001376482.1:c.484A>G	NP_001363411.1:p.Ile162Val
NM_001376483.1:c.484A>G	NP_001363412.1:p.Ile162Val
NM_001376484.1:c.403A>G	NP_001363413.1:p.Ile135Val
NM_015166.4:c.640A>G MANE Select	NP_055981.1:p.Ile214Val
NM_139202.3:c.640A>G	NP_631941.1:p.Ile214Val
NR_164811.1:n.987A>G
NR_164812.1:n.771A>G
NR_164813.1:n.1164A>G