Canonical Allele Identifier: CA359261622

Gene: MYO10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.16670764G>T , CM000667.2:g.16670764G>T	GRCh38
NC_000005.9:g.16670873G>T , CM000667.1:g.16670873G>T	GRCh37
NC_000005.8:g.16723873G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513610.6:c.5645C>A MANE Select	ENSP00000421280.1:p.Thr1882Lys
ENST00000274203.13:c.5678C>A	ENSP00000274203.10:p.Thr1893Lys
ENST00000505695.5:c.3662C>A	ENSP00000421170.1:p.Thr1221Lys
ENST00000513610.5:c.5645C>A	ENSP00000421280.1:p.Thr1882Lys
ENST00000515803.5:c.3662C>A	ENSP00000425051.1:p.Thr1221Lys
NM_012334.2:c.5645C>A	NP_036466.2:p.Thr1882Lys
XM_005248306.3:c.3719C>A	XP_005248363.1:p.Thr1240Lys
XM_005248307.1:c.3716C>A	XP_005248364.1:p.Thr1239Lys
XM_006714475.1:c.5576C>A	XP_006714538.1:p.Thr1859Lys
XM_011514046.1:c.3716C>A	XP_011512348.1:p.Thr1239Lys
XM_005248306.4:c.3719C>A	XP_005248363.1:p.Thr1240Lys
XM_005248307.2:c.3716C>A	XP_005248364.1:p.Thr1239Lys
XM_006714475.3:c.5576C>A	XP_006714538.1:p.Thr1859Lys
XM_011514046.2:c.3716C>A	XP_011512348.1:p.Thr1239Lys
NM_012334.3:c.5645C>A MANE Select	NP_036466.2:p.Thr1882Lys