Canonical Allele Identifier: CA1984131552

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214687C= , CM000673.2:g.77214687C=	GRCh38
NC_000011.9:g.76925732C= , CM000673.1:g.76925732C=	GRCh37
NC_000011.8:g.76603380C=	NCBI36
NG_009086.1:g.91423C=
NG_009086.2:g.91442C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6639C= MANE Select	ENSP00000386331.3:p.Ser2213=
ENST00000670577.1:c.4440C=
ENST00000409619.6:c.6492C=	ENSP00000386635.2:p.Ser2164=
ENST00000409709.7:c.6639C=	ENSP00000386331.3:p.Ser2213=
ENST00000458169.2:c.4065C=	ENSP00000417017.2:p.Ser1355=
ENST00000458637.6:c.6519C=	ENSP00000392185.2:p.Ser2173=
ENST00000481328.7:n.5189C=
ENST00000605744.1:n.2153C=
NM_000260.3:c.6639C=	NP_000251.3:p.Ser2213=
NM_001127180.1:c.6519C=	NP_001120652.1:p.Ser2173=
XM_005274012.2:c.6522C=	XP_005274069.1:p.Ser2174=
XM_006718561.2:c.6525C=	XP_006718624.1:p.Ser2175=
XR_949941.1:n.6933C=
XM_017017780.1:c.6729C=	XP_016873269.1:p.Ser2243=
XM_017017784.1:c.6612C=	XP_016873273.1:p.Ser2204=
XM_017017788.1:c.6615C=	XP_016873277.1:p.Ser2205=
XR_001747885.1:n.6718C=
XR_001747887.1:n.6704C=
NM_000260.4:c.6639C= MANE Select	NP_000251.3:p.Ser2213=
NM_001127180.2:c.6519C=	NP_001120652.1:p.Ser2173=
NM_001369365.1:c.6492C=	NP_001356294.1:p.Ser2164=