Canonical Allele Identifier: CA1207016788

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636238A= , CM000663.2:g.171636238A= GRCh38
NC_000001.10:g.171605378A= , CM000663.1:g.171605378A= GRCh37
NC_000001.9:g.169872001A= NCBI36
NG_008859.1:g.21396T=

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1202T= (MYOC) MANE Select ENSP00000037502.5:p.Ile401=
ENST00000637303.1:c.235-2392A= (MYOCOS) ENSP00000490048.1:n.235-2392A=
ENST00000638471.1:c.*540T= (MYOC) ENSP00000491206.1:n.*540T=
ENST00000037502.10:c.1202T= (MYOC) ENSP00000037502.5:p.Ile401=
ENST00000614688.1:c.*166T= (MYOC) ENSP00000478680.1:n.*166T=
NM_000261.1:c.1202T= (MYOC) NP_000252.1:p.Ile401=
NM_000261.2:c.1202T= (MYOC) MANE Select NP_000252.1:p.Ile401=