Canonical Allele Identifier: CA3210762

Gene: MYO10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.16670845T>A , CM000667.2:g.16670845T>A	GRCh38
NC_000005.9:g.16670954T>A , CM000667.1:g.16670954T>A	GRCh37
NC_000005.8:g.16723954T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513610.6:c.5564A>T MANE Select	ENSP00000421280.1:p.Tyr1855Phe
ENST00000274203.13:c.5597A>T	ENSP00000274203.10:p.Tyr1866Phe
ENST00000505695.5:c.3581A>T	ENSP00000421170.1:p.Tyr1194Phe
ENST00000513610.5:c.5564A>T	ENSP00000421280.1:p.Tyr1855Phe
ENST00000515803.5:c.3581A>T	ENSP00000425051.1:p.Tyr1194Phe
NM_012334.2:c.5564A>T	NP_036466.2:p.Tyr1855Phe
XM_005248306.3:c.3638A>T	XP_005248363.1:p.Tyr1213Phe
XM_005248307.1:c.3635A>T	XP_005248364.1:p.Tyr1212Phe
XM_006714475.1:c.5495A>T	XP_006714538.1:p.Tyr1832Phe
XM_011514046.1:c.3635A>T	XP_011512348.1:p.Tyr1212Phe
XM_005248306.4:c.3638A>T	XP_005248363.1:p.Tyr1213Phe
XM_005248307.2:c.3635A>T	XP_005248364.1:p.Tyr1212Phe
XM_006714475.3:c.5495A>T	XP_006714538.1:p.Tyr1832Phe
XM_011514046.2:c.3635A>T	XP_011512348.1:p.Tyr1212Phe
NM_012334.3:c.5564A>T MANE Select	NP_036466.2:p.Tyr1855Phe