Canonical Allele Identifier: CA1984129913

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211321C= , CM000673.2:g.77211321C=	GRCh38
NC_000011.9:g.76922366C= , CM000673.1:g.76922366C=	GRCh37
NC_000011.8:g.76600014C=	NCBI36
NG_009086.1:g.88057C=
NG_009086.2:g.88076C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6221C= MANE Select	ENSP00000386331.3:p.Pro2074=
ENST00000670577.1:c.4022C=
ENST00000409619.6:c.6074C=	ENSP00000386635.2:p.Pro2025=
ENST00000409709.7:c.6221C=	ENSP00000386331.3:p.Pro2074=
ENST00000458169.2:c.3647C=	ENSP00000417017.2:p.Pro1216=
ENST00000458637.6:c.6107C=	ENSP00000392185.2:p.Pro2036=
ENST00000481328.7:n.3757C=
ENST00000526863.2:n.25+410C=
ENST00000605744.1:n.1688C=
NM_000260.3:c.6221C=	NP_000251.3:p.Pro2074=
NM_001127180.1:c.6107C=	NP_001120652.1:p.Pro2036=
XM_005274012.2:c.6104C=	XP_005274069.1:p.Pro2035=
XM_006718558.2:c.6212C=	XP_006718621.1:p.Pro2071=
XM_006718559.2:c.6107C=	XP_006718622.1:p.Pro2036=
XM_006718560.2:c.6104C=	XP_006718623.1:p.Pro2035=
XM_006718561.2:c.6107C=	XP_006718624.1:p.Pro2036=
XM_011545044.1:c.6221C=	XP_011543346.1:p.Pro2074=
XM_011545045.1:c.6215C=	XP_011543347.1:p.Pro2072=
XM_011545046.1:c.6188C=	XP_011543348.1:p.Pro2063=
XM_011545047.1:c.6125C=	XP_011543349.1:p.Pro2042=
XM_011545048.1:c.5996C=	XP_011543350.1:p.Pro1999=
XM_011545049.1:c.5984C=	XP_011543351.1:p.Pro1995=
XM_011545050.1:c.5957C=	XP_011543352.1:p.Pro1986=
XM_011545051.1:c.6221C=	XP_011543353.1:p.Pro2074=
XR_949938.1:n.6541C=
XR_949941.1:n.6515C=
XM_011545044.2:c.6221C=	XP_011543346.1:p.Pro2074=
XM_011545046.2:c.6311C=	XP_011543348.2:p.Pro2104=
XM_011545050.2:c.5957C=	XP_011543352.1:p.Pro1986=
XM_017017778.1:c.6305C=	XP_016873267.1:p.Pro2102=
XM_017017779.1:c.6302C=	XP_016873268.1:p.Pro2101=
XM_017017780.1:c.6311C=	XP_016873269.1:p.Pro2104=
XM_017017781.1:c.6215C=	XP_016873270.1:p.Pro2072=
XM_017017782.1:c.6197C=	XP_016873271.1:p.Pro2066=
XM_017017783.1:c.6194C=	XP_016873272.1:p.Pro2065=
XM_017017784.1:c.6194C=	XP_016873273.1:p.Pro2065=
XM_017017785.1:c.6074C=	XP_016873274.1:p.Pro2025=
XM_017017786.1:c.6311C=	XP_016873275.1:p.Pro2104=
XM_017017788.1:c.6197C=	XP_016873277.1:p.Pro2066=
XR_001747885.1:n.6300C=
XR_001747887.1:n.6286C=
NM_000260.4:c.6221C= MANE Select	NP_000251.3:p.Pro2074=
NM_001127180.2:c.6107C=	NP_001120652.1:p.Pro2036=
NM_001369365.1:c.6074C=	NP_001356294.1:p.Pro2025=