Canonical Allele Identifier: CA1207016754

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636140C= , CM000663.2:g.171636140C= GRCh38
NC_000001.10:g.171605280C= , CM000663.1:g.171605280C= GRCh37
NC_000001.9:g.169871903C= NCBI36
NG_008859.1:g.21494G=

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1300G= (MYOC) MANE Select ENSP00000037502.5:p.Gly434=
ENST00000637303.1:c.235-2490C= (MYOCOS) ENSP00000490048.1:n.235-2490C=
ENST00000638471.1:c.*638G= (MYOC) ENSP00000491206.1:n.*638G=
ENST00000037502.10:c.1300G= (MYOC) ENSP00000037502.5:p.Gly434=
ENST00000614688.1:c.*264G= (MYOC) ENSP00000478680.1:n.*264G=
NM_000261.1:c.1300G= (MYOC) NP_000252.1:p.Gly434=
NM_000261.2:c.1300G= (MYOC) MANE Select NP_000252.1:p.Gly434=