Canonical Allele Identifier: CA1148281490

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636442C= , CM000663.2:g.171636442C= GRCh38
NC_000001.10:g.171605582C= , CM000663.1:g.171605582C= GRCh37
NC_000001.9:g.169872205C= NCBI36
NG_008859.1:g.21192G=

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.998G= (MYOC) MANE Select ENSP00000037502.5:p.Ser333=
ENST00000637303.1:c.235-2188C= (MYOCOS) ENSP00000490048.1:n.235-2188C=
ENST00000638471.1:c.*336G= (MYOC) ENSP00000491206.1:n.*336G=
ENST00000037502.10:c.998G= (MYOC) ENSP00000037502.5:p.Ser333=
ENST00000614688.1:c.998G= (MYOC) ENSP00000478680.1:p.Ser333=
NM_000261.1:c.998G= (MYOC) NP_000252.1:p.Ser333=
NM_000261.2:c.998G= (MYOC) MANE Select NP_000252.1:p.Ser333=