Canonical Allele Identifier: CA1984131551

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214686G= , CM000673.2:g.77214686G=	GRCh38
NC_000011.9:g.76925731G= , CM000673.1:g.76925731G=	GRCh37
NC_000011.8:g.76603379G=	NCBI36
NG_009086.1:g.91422G=
NG_009086.2:g.91441G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6638G= MANE Select	ENSP00000386331.3:p.Ser2213=
ENST00000670577.1:c.4439G=
ENST00000409619.6:c.6491G=	ENSP00000386635.2:p.Ser2164=
ENST00000409709.7:c.6638G=	ENSP00000386331.3:p.Ser2213=
ENST00000458169.2:c.4064G=	ENSP00000417017.2:p.Ser1355=
ENST00000458637.6:c.6518G=	ENSP00000392185.2:p.Ser2173=
ENST00000481328.7:n.5188G=
ENST00000605744.1:n.2152G=
NM_000260.3:c.6638G=	NP_000251.3:p.Ser2213=
NM_001127180.1:c.6518G=	NP_001120652.1:p.Ser2173=
XM_005274012.2:c.6521G=	XP_005274069.1:p.Ser2174=
XM_006718561.2:c.6524G=	XP_006718624.1:p.Ser2175=
XR_949941.1:n.6932G=
XM_017017780.1:c.6728G=	XP_016873269.1:p.Ser2243=
XM_017017784.1:c.6611G=	XP_016873273.1:p.Ser2204=
XM_017017788.1:c.6614G=	XP_016873277.1:p.Ser2205=
XR_001747885.1:n.6717G=
XR_001747887.1:n.6703G=
NM_000260.4:c.6638G= MANE Select	NP_000251.3:p.Ser2213=
NM_001127180.2:c.6518G=	NP_001120652.1:p.Ser2173=
NM_001369365.1:c.6491G=	NP_001356294.1:p.Ser2164=