Canonical Allele Identifier: CA359262187

Gene: MYO10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.16671465T>C , CM000667.2:g.16671465T>C	GRCh38
NC_000005.9:g.16671574T>C , CM000667.1:g.16671574T>C	GRCh37
NC_000005.8:g.16724574T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513610.6:c.5387A>G MANE Select	ENSP00000421280.1:p.Asn1796Ser
ENST00000274203.13:c.5420A>G	ENSP00000274203.10:p.Asn1807Ser
ENST00000505695.5:c.3404A>G	ENSP00000421170.1:p.Asn1135Ser
ENST00000513610.5:c.5387A>G	ENSP00000421280.1:p.Asn1796Ser
ENST00000515803.5:c.3404A>G	ENSP00000425051.1:p.Asn1135Ser
NM_012334.2:c.5387A>G	NP_036466.2:p.Asn1796Ser
XM_005248306.3:c.3461A>G	XP_005248363.1:p.Asn1154Ser
XM_005248307.1:c.3458A>G	XP_005248364.1:p.Asn1153Ser
XM_006714475.1:c.5318A>G	XP_006714538.1:p.Asn1773Ser
XM_011514046.1:c.3458A>G	XP_011512348.1:p.Asn1153Ser
XM_005248306.4:c.3461A>G	XP_005248363.1:p.Asn1154Ser
XM_005248307.2:c.3458A>G	XP_005248364.1:p.Asn1153Ser
XM_006714475.3:c.5318A>G	XP_006714538.1:p.Asn1773Ser
XM_011514046.2:c.3458A>G	XP_011512348.1:p.Asn1153Ser
NM_012334.3:c.5387A>G MANE Select	NP_036466.2:p.Asn1796Ser