Canonical Allele Identifier: CA1984131521

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214645C= , CM000673.2:g.77214645C=	GRCh38
NC_000011.9:g.76925690C= , CM000673.1:g.76925690C=	GRCh37
NC_000011.8:g.76603338C=	NCBI36
NG_009086.1:g.91381C=
NG_009086.2:g.91400C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6597C= MANE Select	ENSP00000386331.3:p.Ser2199=
ENST00000670577.1:c.4398C=
ENST00000409619.6:c.6450C=	ENSP00000386635.2:p.Ser2150=
ENST00000409709.7:c.6597C=	ENSP00000386331.3:p.Ser2199=
ENST00000458169.2:c.4023C=	ENSP00000417017.2:p.Ser1341=
ENST00000458637.6:c.6477C=	ENSP00000392185.2:p.Ser2159=
ENST00000481328.7:n.5147C=
ENST00000605744.1:n.2111C=
NM_000260.3:c.6597C=	NP_000251.3:p.Ser2199=
NM_001127180.1:c.6477C=	NP_001120652.1:p.Ser2159=
XM_005274012.2:c.6480C=	XP_005274069.1:p.Ser2160=
XM_006718561.2:c.6483C=	XP_006718624.1:p.Ser2161=
XR_949941.1:n.6891C=
XM_017017780.1:c.6687C=	XP_016873269.1:p.Ser2229=
XM_017017784.1:c.6570C=	XP_016873273.1:p.Ser2190=
XM_017017788.1:c.6573C=	XP_016873277.1:p.Ser2191=
XR_001747885.1:n.6676C=
XR_001747887.1:n.6662C=
NM_000260.4:c.6597C= MANE Select	NP_000251.3:p.Ser2199=
NM_001127180.2:c.6477C=	NP_001120652.1:p.Ser2159=
NM_001369365.1:c.6450C=	NP_001356294.1:p.Ser2150=