Canonical Allele Identifier: CA339846032
Gene: MYCL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.39901033G>T , CM000663.2:g.39901033G>T GRCh38
NC_000001.10:g.40366705G>T , CM000663.1:g.40366705G>T GRCh37
NC_000001.9:g.40139292G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000397332.3:c.492C>A ENSP00000380494.2:p.Ser164Arg
ENST00000372816.3:c.402C>A MANE Select ENSP00000361903.2:p.Ser134Arg
ENST00000372815.1:c.492C>A ENSP00000361902.1:p.Ser164Arg
ENST00000372816.2:c.402C>A ENSP00000361903.2:p.Ser134Arg
ENST00000397332.2:c.492C>A ENSP00000380494.2:p.Ser164Arg
NM_001033081.2:c.402C>A NP_001028253.1:p.Ser134Arg
NM_001033082.2:c.492C>A NP_001028254.2:p.Ser164Arg
NM_005376.4:c.492C>A NP_005367.2:p.Ser164Arg
NM_001033081.3:c.402C>A MANE Select NP_001028253.1:p.Ser134Arg
NM_001033082.3:c.492C>A NP_001028254.2:p.Ser164Arg
NM_005376.5:c.492C>A NP_005367.2:p.Ser164Arg