Canonical Allele Identifier: CA1984131592

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214754C= , CM000673.2:g.77214754C=	GRCh38
NC_000011.9:g.76925799C= , CM000673.1:g.76925799C=	GRCh37
NC_000011.8:g.76603447C=	NCBI36
NG_009086.1:g.91490C=
NG_009086.2:g.91509C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.*58C= MANE Select	ENSP00000386331.3:n.*58C=
ENST00000670577.1:c.4507C=
ENST00000409619.6:c.*58C=	ENSP00000386635.2:n.*58C=
ENST00000409709.7:c.*58C=	ENSP00000386331.3:n.*58C=
ENST00000458169.2:c.4132C=	ENSP00000417017.2:n.4132C=
ENST00000458637.6:c.*58C=	ENSP00000392185.2:n.*58C=
ENST00000481328.7:n.5256C=
ENST00000605744.1:n.2220C=
NM_000260.3:c.*58C=	NP_000251.3:n.*58C=
NM_001127180.1:c.*58C=	NP_001120652.1:n.*58C=
XM_005274012.2:c.*58C=	XP_005274069.1:n.*58C=
XM_006718561.2:c.*58C=	XP_006718624.1:n.*58C=
XR_949941.1:n.7000C=
XM_017017780.1:c.*58C=	XP_016873269.1:n.*58C=
XM_017017784.1:c.*58C=	XP_016873273.1:n.*58C=
XM_017017788.1:c.*58C=	XP_016873277.1:n.*58C=
XR_001747885.1:n.6785C=
XR_001747887.1:n.6771C=
NM_000260.4:c.*58C= MANE Select	NP_000251.3:n.*58C=
NM_001127180.2:c.*58C=	NP_001120652.1:n.*58C=
NM_001369365.1:c.*58C=	NP_001356294.1:n.*58C=