Canonical Allele Identifier: CA1207016751

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636137T= , CM000663.2:g.171636137T= GRCh38
NC_000001.10:g.171605277T= , CM000663.1:g.171605277T= GRCh37
NC_000001.9:g.169871900T= NCBI36
NG_008859.1:g.21497A=

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1303A= (MYOC) MANE Select ENSP00000037502.5:p.Thr435=
ENST00000637303.1:c.235-2493T= (MYOCOS) ENSP00000490048.1:n.235-2493T=
ENST00000638471.1:c.*641A= (MYOC) ENSP00000491206.1:n.*641A=
ENST00000037502.10:c.1303A= (MYOC) ENSP00000037502.5:p.Thr435=
ENST00000614688.1:c.*267A= (MYOC) ENSP00000478680.1:n.*267A=
NM_000261.1:c.1303A= (MYOC) NP_000252.1:p.Thr435=
NM_000261.2:c.1303A= (MYOC) MANE Select NP_000252.1:p.Thr435=