Canonical Allele Identifier: CA1140886905

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636010A= , CM000663.2:g.171636010A= GRCh38
NC_000001.10:g.171605150A= , CM000663.1:g.171605150A= GRCh37
NC_000001.9:g.169871773A= NCBI36
NG_008859.1:g.21624T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1430T= (MYOC) MANE Select ENSP00000037502.5:p.Ile477=
ENST00000637303.1:c.235-2620A= (MYOCOS) ENSP00000490048.1:n.235-2620A=
ENST00000638471.1:c.*768T= (MYOC) ENSP00000491206.1:n.*768T=
ENST00000037502.10:c.1430T= (MYOC) ENSP00000037502.5:p.Ile477=
ENST00000614688.1:c.*394T= (MYOC) ENSP00000478680.1:n.*394T=
NM_000261.1:c.1430T= (MYOC) NP_000252.1:p.Ile477=
NM_000261.2:c.1430T= (MYOC) MANE Select NP_000252.1:p.Ile477=