Canonical Allele Identifier: CA381934376

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76919795A>G (hg19) ; chr11:g.77208750A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77208750A>G , CM000673.2:g.77208750A>G	GRCh38
NC_000011.9:g.76919795A>G , CM000673.1:g.76919795A>G	GRCh37
NC_000011.8:g.76597443A>G	NCBI36
NG_009086.1:g.85486A>G
NG_009086.2:g.85505A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5998A>G MANE Select	ENSP00000386331.3:p.Thr2000Ala
ENST00000670577.1:c.3799A>G
ENST00000409619.6:c.5851A>G	ENSP00000386635.2:p.Thr1951Ala
ENST00000409709.7:c.5998A>G	ENSP00000386331.3:p.Thr2000Ala
ENST00000458169.2:c.3424A>G	ENSP00000417017.2:p.Thr1142Ala
ENST00000458637.6:c.5884A>G	ENSP00000392185.2:p.Thr1962Ala
ENST00000481328.7:n.3534A>G
ENST00000605744.1:n.912A>G
NM_000260.3:c.5998A>G	NP_000251.3:p.Thr2000Ala
NM_001127180.1:c.5884A>G	NP_001120652.1:p.Thr1962Ala
XM_005274012.2:c.5881A>G	XP_005274069.1:p.Thr1961Ala
XM_006718558.2:c.5989A>G	XP_006718621.1:p.Thr1997Ala
XM_006718559.2:c.5884A>G	XP_006718622.1:p.Thr1962Ala
XM_006718560.2:c.5881A>G	XP_006718623.1:p.Thr1961Ala
XM_006718561.2:c.5884A>G	XP_006718624.1:p.Thr1962Ala
XM_011545044.1:c.5998A>G	XP_011543346.1:p.Thr2000Ala
XM_011545045.1:c.5992A>G	XP_011543347.1:p.Thr1998Ala
XM_011545046.1:c.5965A>G	XP_011543348.1:p.Thr1989Ala
XM_011545047.1:c.5902A>G	XP_011543349.1:p.Thr1968Ala
XM_011545048.1:c.5773A>G	XP_011543350.1:p.Thr1925Ala
XM_011545049.1:c.5761A>G	XP_011543351.1:p.Thr1921Ala
XM_011545050.1:c.5734A>G	XP_011543352.1:p.Thr1912Ala
XM_011545051.1:c.5998A>G	XP_011543353.1:p.Thr2000Ala
XR_949938.1:n.6318A>G
XR_949941.1:n.6292A>G
XM_011545044.2:c.5998A>G	XP_011543346.1:p.Thr2000Ala
XM_011545046.2:c.6088A>G	XP_011543348.2:p.Thr2030Ala
XM_011545050.2:c.5734A>G	XP_011543352.1:p.Thr1912Ala
XM_017017778.1:c.6082A>G	XP_016873267.1:p.Thr2028Ala
XM_017017779.1:c.6079A>G	XP_016873268.1:p.Thr2027Ala
XM_017017780.1:c.6088A>G	XP_016873269.1:p.Thr2030Ala
XM_017017781.1:c.5992A>G	XP_016873270.1:p.Thr1998Ala
XM_017017782.1:c.5974A>G	XP_016873271.1:p.Thr1992Ala
XM_017017783.1:c.5971A>G	XP_016873272.1:p.Thr1991Ala
XM_017017784.1:c.5971A>G	XP_016873273.1:p.Thr1991Ala
XM_017017785.1:c.5851A>G	XP_016873274.1:p.Thr1951Ala
XM_017017786.1:c.6088A>G	XP_016873275.1:p.Thr2030Ala
XM_017017788.1:c.5974A>G	XP_016873277.1:p.Thr1992Ala
XR_001747885.1:n.6077A>G
XR_001747886.1:n.6018A>G
XR_001747887.1:n.6063A>G
NM_000260.4:c.5998A>G MANE Select	NP_000251.3:p.Thr2000Ala
NM_001127180.2:c.5884A>G	NP_001120652.1:p.Thr1962Ala
NM_001369365.1:c.5851A>G	NP_001356294.1:p.Thr1951Ala