Canonical Allele Identifier: CA339846038
Gene: MYCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39901035T>G , CM000663.2:g.39901035T>G GRCh38
NC_000001.10:g.40366707T>G , CM000663.1:g.40366707T>G GRCh37
NC_000001.9:g.40139294T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397332.3:c.490A>C ENSP00000380494.2:p.Ser164Arg
ENST00000372816.3:c.400A>C MANE Select ENSP00000361903.2:p.Ser134Arg
ENST00000372815.1:c.490A>C ENSP00000361902.1:p.Ser164Arg
ENST00000372816.2:c.400A>C ENSP00000361903.2:p.Ser134Arg
ENST00000397332.2:c.490A>C ENSP00000380494.2:p.Ser164Arg
NM_001033081.2:c.400A>C NP_001028253.1:p.Ser134Arg
NM_001033082.2:c.490A>C NP_001028254.2:p.Ser164Arg
NM_005376.4:c.490A>C NP_005367.2:p.Ser164Arg
NM_001033081.3:c.400A>C MANE Select NP_001028253.1:p.Ser134Arg
NM_001033082.3:c.490A>C NP_001028254.2:p.Ser164Arg
NM_005376.5:c.490A>C NP_005367.2:p.Ser164Arg