Canonical Allele Identifier: CA1362297710

Gene: MYL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46860872_46860873delinsAC , CM000665.2:g.46860872_46860873delinsAC	GRCh38
NC_000003.11:g.46902362_46902363delinsAC , CM000665.1:g.46902362_46902363delinsAC	GRCh37
NC_000003.10:g.46877366_46877367delinsAC	NCBI36
NG_007555.2:g.26297_26298delinsGT , LRG_395:g.26297_26298delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431168.2:c.158-48_158-47delinsGT	ENSP00000393455.2:n.158-48_158-47delinsGT
ENST00000292327.6:c.158-48_158-47delinsGT MANE Select	ENSP00000292327.4:n.158-48_158-47delinsGT
ENST00000653454.1:c.158-48_158-47delinsGT	ENSP00000499624.1:n.158-48_158-47delinsGT
ENST00000654597.1:c.158-48_158-47delinsGT	ENSP00000499406.1:n.158-48_158-47delinsGT
ENST00000655244.1:n.380-48_380-47delinsGT
ENST00000662933.1:c.158-48_158-47delinsGT	ENSP00000499577.1:n.158-48_158-47delinsGT
ENST00000664891.1:n.116-48_116-47delinsGT
ENST00000292327.4:c.158-48_158-47delinsGT	ENSP00000292327.4:n.158-48_158-47delinsGT
ENST00000395869.5:c.158-48_158-47delinsGT	ENSP00000379210.1:n.158-48_158-47delinsGT
NM_000258.2:c.158-48_158-47delinsGT , LRG_395t1:c.158-48_158-47delinsGT	NP_000249.1:n.158-48_158-47delinsGT
NM_000258.3:c.158-48_158-47delinsGT MANE Select	NP_000249.1:n.158-48_158-47delinsGT