Canonical Allele Identifier: CA433474626

Gene: MYL3

Linked Data

• COSMIC: COSM214505
• MyVariant Identifiers: chr3:g.46902291del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46860802del , CM000665.2:g.46860802del	GRCh38
NC_000003.11:g.46902292del , CM000665.1:g.46902292del	GRCh37
NC_000003.10:g.46877296del	NCBI36
NG_007555.2:g.26369del , LRG_395:g.26369del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431168.2:c.182del	ENSP00000393455.2:p.Phe61SerfsTer9
ENST00000292327.6:c.182del MANE Select	ENSP00000292327.4:p.Phe61SerfsTer9
ENST00000653454.1:c.182del	ENSP00000499624.1:p.Phe61SerfsTer9
ENST00000654597.1:c.182del	ENSP00000499406.1:p.Phe61SerfsTer9
ENST00000655244.1:n.404del
ENST00000662933.1:c.182del	ENSP00000499577.1:p.Phe61SerfsTer9
ENST00000664891.1:n.140del
ENST00000292327.4:c.182del	ENSP00000292327.4:p.Phe61SerfsTer9
ENST00000395869.5:c.182del	ENSP00000379210.1:p.Phe61SerfsTer9
NM_000258.2:c.182del , LRG_395t1:c.182del	NP_000249.1:p.Phe61SerfsTer9
NM_000258.3:c.182del MANE Select	NP_000249.1:p.Phe61SerfsTer9