Canonical Allele Identifier: CA73778024

Gene: MYL3

Linked Data

• dbSNP Id: rs879617930
• gnomAD v4: 3-46859448-T-TG
• MyVariant Identifiers: chr3:g.46900938_46900939insG (hg19) ; chr3:g.46859448_46859449insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46859452dup , CM000665.2:g.46859452dup	GRCh38
NC_000003.11:g.46900942dup , CM000665.1:g.46900942dup	GRCh37
NC_000003.10:g.46875946dup	NCBI36
NG_007555.2:g.27721dup , LRG_395:g.27721dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000431168.2:c.481+26dup	ENSP00000393455.2:n.481+26dup
ENST00000292327.6:c.481+26dup MANE Select	ENSP00000292327.4:n.481+26dup
ENST00000653454.1:c.481+26dup	ENSP00000499624.1:n.481+26dup
ENST00000654597.1:c.481+26dup	ENSP00000499406.1:n.481+26dup
ENST00000655244.1:n.703+26dup
ENST00000662933.1:c.481+26dup	ENSP00000499577.1:n.481+26dup
ENST00000664891.1:n.439+26dup
ENST00000292327.4:c.481+26dup	ENSP00000292327.4:n.481+26dup
ENST00000395869.5:c.481+26dup	ENSP00000379210.1:n.481+26dup
NM_000258.2:c.481+26dup , LRG_395t1:c.481+26dup	NP_000249.1:n.481+26dup
NM_000258.3:c.481+26dup MANE Select	NP_000249.1:n.481+26dup