Canonical Allele Identifier: CA1144146963

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635990T= , CM000663.2:g.171635990T= GRCh38
NC_000001.10:g.171605130T= , CM000663.1:g.171605130T= GRCh37
NC_000001.9:g.169871753T= NCBI36
NG_008859.1:g.21644A=

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1450A= (MYOC) MANE Select ENSP00000037502.5:p.Lys484=
ENST00000637303.1:c.235-2640T= (MYOCOS) ENSP00000490048.1:n.235-2640T=
ENST00000638471.1:c.*788A= (MYOC) ENSP00000491206.1:n.*788A=
ENST00000037502.10:c.1450A= (MYOC) ENSP00000037502.5:p.Lys484=
ENST00000614688.1:c.*414A= (MYOC) ENSP00000478680.1:n.*414A=
NM_000261.1:c.1450A= (MYOC) NP_000252.1:p.Lys484=
NM_000261.2:c.1450A= (MYOC) MANE Select NP_000252.1:p.Lys484=