Canonical Allele Identifier: CA3210775

Gene: MYO10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.16670881G>A , CM000667.2:g.16670881G>A	GRCh38
NC_000005.9:g.16670990G>A , CM000667.1:g.16670990G>A	GRCh37
NC_000005.8:g.16723990G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513610.6:c.5528C>T MANE Select	ENSP00000421280.1:p.Thr1843Ile
ENST00000274203.13:c.5561C>T	ENSP00000274203.10:p.Thr1854Ile
ENST00000505695.5:c.3545C>T	ENSP00000421170.1:p.Thr1182Ile
ENST00000513610.5:c.5528C>T	ENSP00000421280.1:p.Thr1843Ile
ENST00000515803.5:c.3545C>T	ENSP00000425051.1:p.Thr1182Ile
NM_012334.2:c.5528C>T	NP_036466.2:p.Thr1843Ile
XM_005248306.3:c.3602C>T	XP_005248363.1:p.Thr1201Ile
XM_005248307.1:c.3599C>T	XP_005248364.1:p.Thr1200Ile
XM_006714475.1:c.5459C>T	XP_006714538.1:p.Thr1820Ile
XM_011514046.1:c.3599C>T	XP_011512348.1:p.Thr1200Ile
XM_005248306.4:c.3602C>T	XP_005248363.1:p.Thr1201Ile
XM_005248307.2:c.3599C>T	XP_005248364.1:p.Thr1200Ile
XM_006714475.3:c.5459C>T	XP_006714538.1:p.Thr1820Ile
XM_011514046.2:c.3599C>T	XP_011512348.1:p.Thr1200Ile
NM_012334.3:c.5528C>T MANE Select	NP_036466.2:p.Thr1843Ile