Canonical Allele Identifier: CA412109345

Gene: MLC1

Linked Data

• ClinVar Variation Id: 553381
• ClinVar RCV Id: RCV000668812
• dbSNP Id: rs281875317
• MyVariant Identifiers: chr22:g.50512725C>G (hg19) ; chr22:g.50074296C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50074296C>G , CM000684.2:g.50074296C>G	GRCh38
NC_000022.10:g.50512725C>G , CM000684.1:g.50512725C>G	GRCh37
NC_000022.9:g.48854852C>G	NCBI36
NG_009162.1:g.16634G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311597.10:c.634G>C MANE Select	ENSP00000310375.6:p.Gly212Arg
ENST00000311597.9:c.634G>C	ENSP00000310375.5:p.Gly212Arg
ENST00000395876.6:c.634G>C	ENSP00000379216.2:p.Gly212Arg
ENST00000442311.1:c.544G>C	ENSP00000401385.1:p.Gly182Arg
ENST00000470008.1:n.114G>C
NM_015166.3:c.634G>C	NP_055981.1:p.Gly212Arg
NM_139202.2:c.634G>C	NP_631941.1:p.Gly212Arg
XM_011530678.1:c.634G>C	XP_011528980.1:p.Gly212Arg
XR_430476.2:n.1029G>C
XM_011530678.2:c.634G>C	XP_011528980.1:p.Gly212Arg
XM_017028671.1:c.634G>C	XP_016884160.1:p.Gly212Arg
XR_001755180.2:n.1139G>C
XR_001755181.2:n.907G>C
NM_001376472.1:c.634G>C	NP_001363401.1:p.Gly212Arg
NM_001376473.1:c.634G>C	NP_001363402.1:p.Gly212Arg
NM_001376474.1:c.634G>C	NP_001363403.1:p.Gly212Arg
NM_001376475.1:c.634G>C	NP_001363404.1:p.Gly212Arg
NM_001376476.1:c.634G>C	NP_001363405.1:p.Gly212Arg
NM_001376477.1:c.634G>C	NP_001363406.1:p.Gly212Arg
NM_001376478.1:c.634G>C	NP_001363407.1:p.Gly212Arg
NM_001376479.1:c.634G>C	NP_001363408.1:p.Gly212Arg
NM_001376480.1:c.544G>C	NP_001363409.1:p.Gly182Arg
NM_001376481.1:c.532G>C	NP_001363410.1:p.Gly178Arg
NM_001376482.1:c.478G>C	NP_001363411.1:p.Gly160Arg
NM_001376483.1:c.478G>C	NP_001363412.1:p.Gly160Arg
NM_001376484.1:c.397G>C	NP_001363413.1:p.Gly133Arg
NM_015166.4:c.634G>C MANE Select	NP_055981.1:p.Gly212Arg
NM_139202.3:c.634G>C	NP_631941.1:p.Gly212Arg
NR_164811.1:n.981G>C
NR_164812.1:n.765G>C
NR_164813.1:n.1158G>C