Canonical Allele Identifier: CA2665478613

Gene: MYL3

Linked Data

• gnomAD v4: 3-46860595-TATCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46860596_46860599del , CM000665.2:g.46860596_46860599del	GRCh38
NC_000003.11:g.46902086_46902089del , CM000665.1:g.46902086_46902089del	GRCh37
NC_000003.10:g.46877090_46877093del	NCBI36
NG_007555.2:g.26571_26574del , LRG_395:g.26571_26574del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000431168.2:c.307+77_307+80del	ENSP00000393455.2:n.307+77_307+80del
ENST00000292327.6:c.307+77_307+80del MANE Select	ENSP00000292327.4:n.307+77_307+80del
ENST00000653454.1:c.307+77_307+80del	ENSP00000499624.1:n.307+77_307+80del
ENST00000654597.1:c.307+77_307+80del	ENSP00000499406.1:n.307+77_307+80del
ENST00000655244.1:n.529+77_529+80del
ENST00000662933.1:c.307+77_307+80del	ENSP00000499577.1:n.307+77_307+80del
ENST00000664891.1:n.265+77_265+80del
ENST00000292327.4:c.307+77_307+80del	ENSP00000292327.4:n.307+77_307+80del
ENST00000395869.5:c.307+77_307+80del	ENSP00000379210.1:n.307+77_307+80del
NM_000258.2:c.307+77_307+80del , LRG_395t1:c.307+77_307+80del	NP_000249.1:n.307+77_307+80del
NM_000258.3:c.307+77_307+80del MANE Select	NP_000249.1:n.307+77_307+80del