Canonical Allele Identifier: CA343723562

Linked Data

ClinVar Variation Id: 2575101
ClinVar RCV Id: RCV003320026

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636076G>T , CM000663.2:g.171636076G>T GRCh38
NC_000001.10:g.171605216G>T , CM000663.1:g.171605216G>T GRCh37
NC_000001.9:g.169871839G>T NCBI36
NG_008859.1:g.21558C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1364C>A (MYOC) MANE Select ENSP00000037502.5:p.Thr455Lys
ENST00000637303.1:c.235-2554G>T (MYOCOS) ENSP00000490048.1:n.235-2554G>T
ENST00000638471.1:c.*702C>A (MYOC) ENSP00000491206.1:n.*702C>A
ENST00000037502.10:c.1364C>A (MYOC) ENSP00000037502.5:p.Thr455Lys
ENST00000614688.1:c.*328C>A (MYOC) ENSP00000478680.1:n.*328C>A
NM_000261.1:c.1364C>A (MYOC) NP_000252.1:p.Thr455Lys
NM_000261.2:c.1364C>A (MYOC) MANE Select NP_000252.1:p.Thr455Lys