Canonical Allele Identifier: CA2044298672
Gene: LYZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69350132G= , CM000674.2:g.69350132G= GRCh38
NC_000012.11:g.69743912G= , CM000674.1:g.69743912G= GRCh37
NC_000012.10:g.68030179G= NCBI36
NG_008195.1:g.6779G= , LRG_768:g.6779G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261267.7:c.161G= MANE Select ENSP00000261267.2:p.Ser54=
ENST00000261267.6:c.161G= ENSP00000261267.2:p.Ser54=
ENST00000548839.1:c.161G= ENSP00000449969.1:p.Ser54=
ENST00000549690.1:c.161G= ENSP00000449898.1:p.Ser54=
NM_000239.2:c.161G= , LRG_768t1:c.161G= NP_000230.1:p.Ser54=
NM_000239.3:c.161G= MANE Select NP_000230.1:p.Ser54=