Canonical Allele Identifier: CA1207016628

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635754A= , CM000663.2:g.171635754A= GRCh38
NC_000001.10:g.171604894A= , CM000663.1:g.171604894A= GRCh37
NC_000001.9:g.169871517A= NCBI36
NG_008859.1:g.21880T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*171T= (MYOC) MANE Select ENSP00000037502.5:n.*171T=
ENST00000637303.1:c.235-2876A= (MYOCOS) ENSP00000490048.1:n.235-2876A=
ENST00000638471.1:c.*1024T= (MYOC) ENSP00000491206.1:n.*1024T=
ENST00000037502.10:c.*171T= (MYOC) ENSP00000037502.5:n.*171T=
ENST00000614688.1:c.*650T= (MYOC) ENSP00000478680.1:n.*650T=
NM_000261.1:c.*171T= (MYOC) NP_000252.1:n.*171T=
NM_000261.2:c.*171T= (MYOC) MANE Select NP_000252.1:n.*171T=