Canonical Allele Identifier: CA645978168

Gene: MYOC MYOCOS

Linked Data

• COSMIC: COSN20263902

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171635572_171635573insC , CM000663.2:g.171635572_171635573insC	GRCh38
NC_000001.10:g.171604712_171604713insC , CM000663.1:g.171604712_171604713insC	GRCh37
NC_000001.9:g.169871335_169871336insC	NCBI36
NG_008859.1:g.22061_22062insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000037502.11:c.*352_*353insG (MYOC) MANE Select	ENSP00000037502.5:n.*352_*353insG
ENST00000637303.1:c.235-3058_235-3057insC (MYOCOS)	ENSP00000490048.1:n.235-3058_235-3057insC
ENST00000638471.1:c.*1205_*1206insG (MYOC)	ENSP00000491206.1:n.*1205_*1206insG
ENST00000037502.10:c.*352_*353insG (MYOC)	ENSP00000037502.5:n.*352_*353insG
ENST00000614688.1:c.*831_*832insG (MYOC)	ENSP00000478680.1:n.*831_*832insG
NM_000261.1:c.*352_*353insG (MYOC)	NP_000252.1:n.*352_*353insG
NM_000261.2:c.*352_*353insG (MYOC) MANE Select	NP_000252.1:n.*352_*353insG