Canonical Allele Identifier: CA381954088

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76918413A>G (hg19) ; chr11:g.77207368A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207368A>G , CM000673.2:g.77207368A>G	GRCh38
NC_000011.9:g.76918413A>G , CM000673.1:g.76918413A>G	GRCh37
NC_000011.8:g.76596061A>G	NCBI36
NG_009086.1:g.84104A>G
NG_009086.2:g.84123A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5822A>G MANE Select	ENSP00000386331.3:p.Glu1941Gly
ENST00000670577.1:c.3649A>G
ENST00000409619.6:c.5675A>G	ENSP00000386635.2:p.Glu1892Gly
ENST00000409709.7:c.5822A>G	ENSP00000386331.3:p.Glu1941Gly
ENST00000458169.2:c.3248A>G	ENSP00000417017.2:p.Glu1083Gly
ENST00000458637.6:c.5708A>G	ENSP00000392185.2:p.Glu1903Gly
ENST00000481328.7:n.3358A>G
ENST00000605744.1:n.736A>G
NM_000260.3:c.5822A>G	NP_000251.3:p.Glu1941Gly
NM_001127180.1:c.5708A>G	NP_001120652.1:p.Glu1903Gly
XM_005274012.2:c.5705A>G	XP_005274069.1:p.Glu1902Gly
XM_006718558.2:c.5813A>G	XP_006718621.1:p.Glu1938Gly
XM_006718559.2:c.5708A>G	XP_006718622.1:p.Glu1903Gly
XM_006718560.2:c.5705A>G	XP_006718623.1:p.Glu1902Gly
XM_006718561.2:c.5708A>G	XP_006718624.1:p.Glu1903Gly
XM_011545044.1:c.5822A>G	XP_011543346.1:p.Glu1941Gly
XM_011545045.1:c.5816A>G	XP_011543347.1:p.Glu1939Gly
XM_011545046.1:c.5789A>G	XP_011543348.1:p.Glu1930Gly
XM_011545047.1:c.5726A>G	XP_011543349.1:p.Glu1909Gly
XM_011545048.1:c.5597A>G	XP_011543350.1:p.Glu1866Gly
XM_011545049.1:c.5585A>G	XP_011543351.1:p.Glu1862Gly
XM_011545050.1:c.5558A>G	XP_011543352.1:p.Glu1853Gly
XM_011545051.1:c.5822A>G	XP_011543353.1:p.Glu1941Gly
XR_949938.1:n.6142A>G
XR_949941.1:n.6142A>G
XM_011545044.2:c.5822A>G	XP_011543346.1:p.Glu1941Gly
XM_011545046.2:c.5912A>G	XP_011543348.2:p.Glu1971Gly
XM_011545050.2:c.5558A>G	XP_011543352.1:p.Glu1853Gly
XM_017017778.1:c.5906A>G	XP_016873267.1:p.Glu1969Gly
XM_017017779.1:c.5903A>G	XP_016873268.1:p.Glu1968Gly
XM_017017780.1:c.5912A>G	XP_016873269.1:p.Glu1971Gly
XM_017017781.1:c.5816A>G	XP_016873270.1:p.Glu1939Gly
XM_017017782.1:c.5798A>G	XP_016873271.1:p.Glu1933Gly
XM_017017783.1:c.5795A>G	XP_016873272.1:p.Glu1932Gly
XM_017017784.1:c.5795A>G	XP_016873273.1:p.Glu1932Gly
XM_017017785.1:c.5675A>G	XP_016873274.1:p.Glu1892Gly
XM_017017786.1:c.5912A>G	XP_016873275.1:p.Glu1971Gly
XM_017017788.1:c.5798A>G	XP_016873277.1:p.Glu1933Gly
XR_001747885.1:n.5927A>G
XR_001747886.1:n.5842A>G
XR_001747887.1:n.5913A>G
NM_000260.4:c.5822A>G MANE Select	NP_000251.3:p.Glu1941Gly
NM_001127180.2:c.5708A>G	NP_001120652.1:p.Glu1903Gly
NM_001369365.1:c.5675A>G	NP_001356294.1:p.Glu1892Gly