Canonical Allele Identifier: CA3210958

Gene: MYO10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.16673850G>A , CM000667.2:g.16673850G>A	GRCh38
NC_000005.9:g.16673959G>A , CM000667.1:g.16673959G>A	GRCh37
NC_000005.8:g.16726959G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513610.6:c.5004C>T MANE Select	ENSP00000421280.1:p.Tyr1668=
ENST00000274203.13:c.5037C>T	ENSP00000274203.10:p.Tyr1679=
ENST00000505695.5:c.3021C>T	ENSP00000421170.1:p.Tyr1007=
ENST00000513610.5:c.5004C>T	ENSP00000421280.1:p.Tyr1668=
ENST00000515803.5:c.3021C>T	ENSP00000425051.1:p.Tyr1007=
NM_012334.2:c.5004C>T	NP_036466.2:p.Tyr1668=
XM_005248306.3:c.3078C>T	XP_005248363.1:p.Tyr1026=
XM_005248307.1:c.3075C>T	XP_005248364.1:p.Tyr1025=
XM_006714475.1:c.4935C>T	XP_006714538.1:p.Tyr1645=
XM_011514046.1:c.3075C>T	XP_011512348.1:p.Tyr1025=
XM_005248306.4:c.3078C>T	XP_005248363.1:p.Tyr1026=
XM_005248307.2:c.3075C>T	XP_005248364.1:p.Tyr1025=
XM_006714475.3:c.4935C>T	XP_006714538.1:p.Tyr1645=
XM_011514046.2:c.3075C>T	XP_011512348.1:p.Tyr1025=
NM_012334.3:c.5004C>T MANE Select	NP_036466.2:p.Tyr1668=