Canonical Allele Identifier: CA381934718

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76919837C>G (hg19) ; chr11:g.77208792C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77208792C>G , CM000673.2:g.77208792C>G	GRCh38
NC_000011.9:g.76919837C>G , CM000673.1:g.76919837C>G	GRCh37
NC_000011.8:g.76597485C>G	NCBI36
NG_009086.1:g.85528C>G
NG_009086.2:g.85547C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.6040C>G MANE Select	ENSP00000386331.3:p.His2014Asp
ENST00000670577.1:c.3841C>G
ENST00000409619.6:c.5893C>G	ENSP00000386635.2:p.His1965Asp
ENST00000409709.7:c.6040C>G	ENSP00000386331.3:p.His2014Asp
ENST00000458169.2:c.3466C>G	ENSP00000417017.2:p.His1156Asp
ENST00000458637.6:c.5926C>G	ENSP00000392185.2:p.His1976Asp
ENST00000481328.7:n.3576C>G
ENST00000605744.1:n.954C>G
NM_000260.3:c.6040C>G	NP_000251.3:p.His2014Asp
NM_001127180.1:c.5926C>G	NP_001120652.1:p.His1976Asp
XM_005274012.2:c.5923C>G	XP_005274069.1:p.His1975Asp
XM_006718558.2:c.6031C>G	XP_006718621.1:p.His2011Asp
XM_006718559.2:c.5926C>G	XP_006718622.1:p.His1976Asp
XM_006718560.2:c.5923C>G	XP_006718623.1:p.His1975Asp
XM_006718561.2:c.5926C>G	XP_006718624.1:p.His1976Asp
XM_011545044.1:c.6040C>G	XP_011543346.1:p.His2014Asp
XM_011545045.1:c.6034C>G	XP_011543347.1:p.His2012Asp
XM_011545046.1:c.6007C>G	XP_011543348.1:p.His2003Asp
XM_011545047.1:c.5944C>G	XP_011543349.1:p.His1982Asp
XM_011545048.1:c.5815C>G	XP_011543350.1:p.His1939Asp
XM_011545049.1:c.5803C>G	XP_011543351.1:p.His1935Asp
XM_011545050.1:c.5776C>G	XP_011543352.1:p.His1926Asp
XM_011545051.1:c.6040C>G	XP_011543353.1:p.His2014Asp
XR_949938.1:n.6360C>G
XR_949941.1:n.6334C>G
XM_011545044.2:c.6040C>G	XP_011543346.1:p.His2014Asp
XM_011545046.2:c.6130C>G	XP_011543348.2:p.His2044Asp
XM_011545050.2:c.5776C>G	XP_011543352.1:p.His1926Asp
XM_017017778.1:c.6124C>G	XP_016873267.1:p.His2042Asp
XM_017017779.1:c.6121C>G	XP_016873268.1:p.His2041Asp
XM_017017780.1:c.6130C>G	XP_016873269.1:p.His2044Asp
XM_017017781.1:c.6034C>G	XP_016873270.1:p.His2012Asp
XM_017017782.1:c.6016C>G	XP_016873271.1:p.His2006Asp
XM_017017783.1:c.6013C>G	XP_016873272.1:p.His2005Asp
XM_017017784.1:c.6013C>G	XP_016873273.1:p.His2005Asp
XM_017017785.1:c.5893C>G	XP_016873274.1:p.His1965Asp
XM_017017786.1:c.6130C>G	XP_016873275.1:p.His2044Asp
XM_017017788.1:c.6016C>G	XP_016873277.1:p.His2006Asp
XR_001747885.1:n.6119C>G
XR_001747886.1:n.6060C>G
XR_001747887.1:n.6105C>G
NM_000260.4:c.6040C>G MANE Select	NP_000251.3:p.His2014Asp
NM_001127180.2:c.5926C>G	NP_001120652.1:p.His1976Asp
NM_001369365.1:c.5893C>G	NP_001356294.1:p.His1965Asp