Canonical Allele Identifier: CA381953861

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76918344T>G (hg19) ; chr11:g.77207299T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207299T>G , CM000673.2:g.77207299T>G	GRCh38
NC_000011.9:g.76918344T>G , CM000673.1:g.76918344T>G	GRCh37
NC_000011.8:g.76595992T>G	NCBI36
NG_009086.1:g.84035T>G
NG_009086.2:g.84054T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5753T>G MANE Select	ENSP00000386331.3:p.Val1918Gly
ENST00000670577.1:c.3580T>G
ENST00000409619.6:c.5606T>G	ENSP00000386635.2:p.Val1869Gly
ENST00000409709.7:c.5753T>G	ENSP00000386331.3:p.Val1918Gly
ENST00000458169.2:c.3179T>G	ENSP00000417017.2:p.Val1060Gly
ENST00000458637.6:c.5639T>G	ENSP00000392185.2:p.Val1880Gly
ENST00000481328.7:n.3289T>G
ENST00000605744.1:n.667T>G
NM_000260.3:c.5753T>G	NP_000251.3:p.Val1918Gly
NM_001127180.1:c.5639T>G	NP_001120652.1:p.Val1880Gly
XM_005274012.2:c.5636T>G	XP_005274069.1:p.Val1879Gly
XM_006718558.2:c.5744T>G	XP_006718621.1:p.Val1915Gly
XM_006718559.2:c.5639T>G	XP_006718622.1:p.Val1880Gly
XM_006718560.2:c.5636T>G	XP_006718623.1:p.Val1879Gly
XM_006718561.2:c.5639T>G	XP_006718624.1:p.Val1880Gly
XM_011545044.1:c.5753T>G	XP_011543346.1:p.Val1918Gly
XM_011545045.1:c.5747T>G	XP_011543347.1:p.Val1916Gly
XM_011545046.1:c.5720T>G	XP_011543348.1:p.Val1907Gly
XM_011545047.1:c.5657T>G	XP_011543349.1:p.Val1886Gly
XM_011545048.1:c.5528T>G	XP_011543350.1:p.Val1843Gly
XM_011545049.1:c.5516T>G	XP_011543351.1:p.Val1839Gly
XM_011545050.1:c.5489T>G	XP_011543352.1:p.Val1830Gly
XM_011545051.1:c.5753T>G	XP_011543353.1:p.Val1918Gly
XR_949938.1:n.6073T>G
XR_949941.1:n.6073T>G
XM_011545044.2:c.5753T>G	XP_011543346.1:p.Val1918Gly
XM_011545046.2:c.5843T>G	XP_011543348.2:p.Val1948Gly
XM_011545050.2:c.5489T>G	XP_011543352.1:p.Val1830Gly
XM_017017778.1:c.5837T>G	XP_016873267.1:p.Val1946Gly
XM_017017779.1:c.5834T>G	XP_016873268.1:p.Val1945Gly
XM_017017780.1:c.5843T>G	XP_016873269.1:p.Val1948Gly
XM_017017781.1:c.5747T>G	XP_016873270.1:p.Val1916Gly
XM_017017782.1:c.5729T>G	XP_016873271.1:p.Val1910Gly
XM_017017783.1:c.5726T>G	XP_016873272.1:p.Val1909Gly
XM_017017784.1:c.5726T>G	XP_016873273.1:p.Val1909Gly
XM_017017785.1:c.5606T>G	XP_016873274.1:p.Val1869Gly
XM_017017786.1:c.5843T>G	XP_016873275.1:p.Val1948Gly
XM_017017788.1:c.5729T>G	XP_016873277.1:p.Val1910Gly
XR_001747885.1:n.5858T>G
XR_001747886.1:n.5773T>G
XR_001747887.1:n.5844T>G
NM_000260.4:c.5753T>G MANE Select	NP_000251.3:p.Val1918Gly
NM_001127180.2:c.5639T>G	NP_001120652.1:p.Val1880Gly
NM_001369365.1:c.5606T>G	NP_001356294.1:p.Val1869Gly