Canonical Allele Identifier: CA2063066351
Gene: MYL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.110910995_110910998delinsCAGA , CM000674.2:g.110910995_110910998delinsCAGA GRCh38
NC_000012.11:g.111348799_111348802delinsCAGA , CM000674.1:g.111348799_111348802delinsCAGA GRCh37
NC_000012.10:g.109833182_109833185delinsCAGA NCBI36
NG_007554.1:g.14580_14583delinsTCTG , LRG_393:g.14580_14583delinsTCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000228841.15:c.*79_*82delinsTCTG MANE Select ENSP00000228841.8:n.*79_*82delinsTCTG
ENST00000663220.1:c.*79_*82delinsTCTG ENSP00000499568.1:n.*79_*82delinsTCTG
ENST00000228841.12:c.*79_*82delinsTCTG ENSP00000228841.7:n.*79_*82delinsTCTG
ENST00000548438.1:c.*79_*82delinsTCTG ENSP00000447154.1:n.*79_*82delinsTCTG
NM_000432.3:c.*79_*82delinsTCTG , LRG_393t1:c.*79_*82delinsTCTG NP_000423.2:n.*79_*82delinsTCTG
NM_000432.4:c.*79_*82delinsTCTG MANE Select NP_000423.2:n.*79_*82delinsTCTG