Canonical Allele Identifier: CA515002431
Gene: MLC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.50523161C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50084732C>G , CM000684.2:g.50084732C>G GRCh38
NC_000022.10:g.50523161C>G , CM000684.1:g.50523161C>G GRCh37
NC_000022.9:g.48865288C>G NCBI36
NG_009162.1:g.6198G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000311597.10:c.171G>C MANE Select ENSP00000310375.6:p.Leu57=
ENST00000311597.9:c.171G>C ENSP00000310375.5:p.Leu57=
ENST00000395876.6:c.171G>C ENSP00000379216.2:p.Leu57=
ENST00000442311.1:c.171G>C ENSP00000401385.1:p.Leu57=
NM_015166.3:c.171G>C NP_055981.1:p.Leu57=
NM_139202.2:c.171G>C NP_631941.1:p.Leu57=
XM_011530678.1:c.171G>C XP_011528980.1:p.Leu57=
XR_430476.2:n.566G>C
XM_011530678.2:c.171G>C XP_011528980.1:p.Leu57=
XM_017028671.1:c.171G>C XP_016884160.1:p.Leu57=
XR_001755180.2:n.676G>C
XR_001755181.2:n.444G>C
NM_001376472.1:c.171G>C NP_001363401.1:p.Leu57=
NM_001376473.1:c.171G>C NP_001363402.1:p.Leu57=
NM_001376474.1:c.171G>C NP_001363403.1:p.Leu57=
NM_001376475.1:c.171G>C NP_001363404.1:p.Leu57=
NM_001376476.1:c.171G>C NP_001363405.1:p.Leu57=
NM_001376477.1:c.171G>C NP_001363406.1:p.Leu57=
NM_001376478.1:c.171G>C NP_001363407.1:p.Leu57=
NM_001376479.1:c.171G>C NP_001363408.1:p.Leu57=
NM_001376480.1:c.171G>C NP_001363409.1:p.Leu57=
NM_001376481.1:c.171G>C NP_001363410.1:p.Leu57=
NM_001376482.1:c.171G>C NP_001363411.1:p.Leu57=
NM_001376483.1:c.171G>C NP_001363412.1:p.Leu57=
NM_001376484.1:c.-59+623G>C NP_001363413.1:n.-59+623G>C
NM_015166.4:c.171G>C MANE Select NP_055981.1:p.Leu57=
NM_139202.3:c.171G>C NP_631941.1:p.Leu57=
NR_164811.1:n.518G>C
NR_164812.1:n.302G>C
NR_164813.1:n.695G>C