Canonical Allele Identifier: CA381953827

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76918337T>A (hg19) ; chr11:g.77207292T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207292T>A , CM000673.2:g.77207292T>A	GRCh38
NC_000011.9:g.76918337T>A , CM000673.1:g.76918337T>A	GRCh37
NC_000011.8:g.76595985T>A	NCBI36
NG_009086.1:g.84028T>A
NG_009086.2:g.84047T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5746T>A MANE Select	ENSP00000386331.3:p.Phe1916Ile
ENST00000670577.1:c.3573T>A
ENST00000409619.6:c.5599T>A	ENSP00000386635.2:p.Phe1867Ile
ENST00000409709.7:c.5746T>A	ENSP00000386331.3:p.Phe1916Ile
ENST00000458169.2:c.3172T>A	ENSP00000417017.2:p.Phe1058Ile
ENST00000458637.6:c.5632T>A	ENSP00000392185.2:p.Phe1878Ile
ENST00000481328.7:n.3282T>A
ENST00000605744.1:n.660T>A
NM_000260.3:c.5746T>A	NP_000251.3:p.Phe1916Ile
NM_001127180.1:c.5632T>A	NP_001120652.1:p.Phe1878Ile
XM_005274012.2:c.5629T>A	XP_005274069.1:p.Phe1877Ile
XM_006718558.2:c.5737T>A	XP_006718621.1:p.Phe1913Ile
XM_006718559.2:c.5632T>A	XP_006718622.1:p.Phe1878Ile
XM_006718560.2:c.5629T>A	XP_006718623.1:p.Phe1877Ile
XM_006718561.2:c.5632T>A	XP_006718624.1:p.Phe1878Ile
XM_011545044.1:c.5746T>A	XP_011543346.1:p.Phe1916Ile
XM_011545045.1:c.5740T>A	XP_011543347.1:p.Phe1914Ile
XM_011545046.1:c.5713T>A	XP_011543348.1:p.Phe1905Ile
XM_011545047.1:c.5650T>A	XP_011543349.1:p.Phe1884Ile
XM_011545048.1:c.5521T>A	XP_011543350.1:p.Phe1841Ile
XM_011545049.1:c.5509T>A	XP_011543351.1:p.Phe1837Ile
XM_011545050.1:c.5482T>A	XP_011543352.1:p.Phe1828Ile
XM_011545051.1:c.5746T>A	XP_011543353.1:p.Phe1916Ile
XR_949938.1:n.6066T>A
XR_949941.1:n.6066T>A
XM_011545044.2:c.5746T>A	XP_011543346.1:p.Phe1916Ile
XM_011545046.2:c.5836T>A	XP_011543348.2:p.Phe1946Ile
XM_011545050.2:c.5482T>A	XP_011543352.1:p.Phe1828Ile
XM_017017778.1:c.5830T>A	XP_016873267.1:p.Phe1944Ile
XM_017017779.1:c.5827T>A	XP_016873268.1:p.Phe1943Ile
XM_017017780.1:c.5836T>A	XP_016873269.1:p.Phe1946Ile
XM_017017781.1:c.5740T>A	XP_016873270.1:p.Phe1914Ile
XM_017017782.1:c.5722T>A	XP_016873271.1:p.Phe1908Ile
XM_017017783.1:c.5719T>A	XP_016873272.1:p.Phe1907Ile
XM_017017784.1:c.5719T>A	XP_016873273.1:p.Phe1907Ile
XM_017017785.1:c.5599T>A	XP_016873274.1:p.Phe1867Ile
XM_017017786.1:c.5836T>A	XP_016873275.1:p.Phe1946Ile
XM_017017788.1:c.5722T>A	XP_016873277.1:p.Phe1908Ile
XR_001747885.1:n.5851T>A
XR_001747886.1:n.5766T>A
XR_001747887.1:n.5837T>A
NM_000260.4:c.5746T>A MANE Select	NP_000251.3:p.Phe1916Ile
NM_001127180.2:c.5632T>A	NP_001120652.1:p.Phe1878Ile
NM_001369365.1:c.5599T>A	NP_001356294.1:p.Phe1867Ile