Canonical Allele Identifier: CA655326843

Gene: MYL2

Linked Data

• COSMIC: COSN20493962

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.110910911_110910912insT , CM000674.2:g.110910911_110910912insT	GRCh38
NC_000012.11:g.111348715_111348716insT , CM000674.1:g.111348715_111348716insT	GRCh37
NC_000012.10:g.109833098_109833099insT	NCBI36
NG_007554.1:g.14666_14667insA , LRG_393:g.14666_14667insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000228841.15:c.*165_*166insA MANE Select	ENSP00000228841.8:n.*165_*166insA
ENST00000663220.1:c.*165_*166insA	ENSP00000499568.1:n.*165_*166insA
ENST00000228841.12:c.*165_*166insA	ENSP00000228841.7:n.*165_*166insA
NM_000432.3:c.*165_*166insA , LRG_393t1:c.*165_*166insA	NP_000423.2:n.*165_*166insA
NM_000432.4:c.*165_*166insA MANE Select	NP_000423.2:n.*165_*166insA