Canonical Allele Identifier: CA1984122690

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77199685C= , CM000673.2:g.77199685C=	GRCh38
NC_000011.9:g.76910730C= , CM000673.1:g.76910730C=	GRCh37
NC_000011.8:g.76588378C=	NCBI36
NG_009086.1:g.76421C=
NG_009086.2:g.76440C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.4719C= MANE Select	ENSP00000386331.3:p.Ala1573=
ENST00000670577.1:c.2560C=
ENST00000409619.6:c.4572C=	ENSP00000386635.2:p.Ala1524=
ENST00000409709.7:c.4719C=	ENSP00000386331.3:p.Ala1573=
ENST00000458169.2:c.2148C=	ENSP00000417017.2:p.Ala716=
ENST00000458637.6:c.4605C=	ENSP00000392185.2:p.Ala1535=
ENST00000481328.7:n.2258C=
NM_000260.3:c.4719C=	NP_000251.3:p.Ala1573=
NM_001127180.1:c.4605C=	NP_001120652.1:p.Ala1535=
XM_005274012.2:c.4605C=	XP_005274069.1:p.Ala1535=
XM_006718558.2:c.4713C=	XP_006718621.1:p.Ala1571=
XM_006718559.2:c.4605C=	XP_006718622.1:p.Ala1535=
XM_006718560.2:c.4605C=	XP_006718623.1:p.Ala1535=
XM_006718561.2:c.4605C=	XP_006718624.1:p.Ala1535=
XM_011545044.1:c.4719C=	XP_011543346.1:p.Ala1573=
XM_011545045.1:c.4713C=	XP_011543347.1:p.Ala1571=
XM_011545046.1:c.4686C=	XP_011543348.1:p.Ala1562=
XM_011545047.1:c.4623C=	XP_011543349.1:p.Ala1541=
XM_011545048.1:c.4494C=	XP_011543350.1:p.Ala1498=
XM_011545049.1:c.4482C=	XP_011543351.1:p.Ala1494=
XM_011545050.1:c.4455C=	XP_011543352.1:p.Ala1485=
XM_011545051.1:c.4719C=	XP_011543353.1:p.Ala1573=
XM_011545052.1:c.4719C=	XP_011543354.1:p.Ala1573=
XR_949938.1:n.5039C=
XR_949941.1:n.5039C=
XR_949942.1:n.5041C=
XM_011545044.2:c.4719C=	XP_011543346.1:p.Ala1573=
XM_011545046.2:c.4809C=	XP_011543348.2:p.Ala1603=
XM_011545050.2:c.4455C=	XP_011543352.1:p.Ala1485=
XM_017017778.1:c.4803C=	XP_016873267.1:p.Ala1601=
XM_017017779.1:c.4803C=	XP_016873268.1:p.Ala1601=
XM_017017780.1:c.4809C=	XP_016873269.1:p.Ala1603=
XM_017017781.1:c.4713C=	XP_016873270.1:p.Ala1571=
XM_017017782.1:c.4695C=	XP_016873271.1:p.Ala1565=
XM_017017783.1:c.4695C=	XP_016873272.1:p.Ala1565=
XM_017017784.1:c.4695C=	XP_016873273.1:p.Ala1565=
XM_017017785.1:c.4572C=	XP_016873274.1:p.Ala1524=
XM_017017786.1:c.4809C=	XP_016873275.1:p.Ala1603=
XM_017017788.1:c.4695C=	XP_016873277.1:p.Ala1565=
XR_001747885.1:n.4824C=
XR_001747886.1:n.4824C=
XR_001747887.1:n.4824C=
XR_001747888.1:n.4824C=
NM_000260.4:c.4719C= MANE Select	NP_000251.3:p.Ala1573=
NM_001127180.2:c.4605C=	NP_001120652.1:p.Ala1535=
NM_001369365.1:c.4572C=	NP_001356294.1:p.Ala1524=