Canonical Allele Identifier: CA381954062

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76918401T>G (hg19) ; chr11:g.77207356T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207356T>G , CM000673.2:g.77207356T>G	GRCh38
NC_000011.9:g.76918401T>G , CM000673.1:g.76918401T>G	GRCh37
NC_000011.8:g.76596049T>G	NCBI36
NG_009086.1:g.84092T>G
NG_009086.2:g.84111T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5810T>G MANE Select	ENSP00000386331.3:p.Leu1937Arg
ENST00000670577.1:c.3637T>G
ENST00000409619.6:c.5663T>G	ENSP00000386635.2:p.Leu1888Arg
ENST00000409709.7:c.5810T>G	ENSP00000386331.3:p.Leu1937Arg
ENST00000458169.2:c.3236T>G	ENSP00000417017.2:p.Leu1079Arg
ENST00000458637.6:c.5696T>G	ENSP00000392185.2:p.Leu1899Arg
ENST00000481328.7:n.3346T>G
ENST00000605744.1:n.724T>G
NM_000260.3:c.5810T>G	NP_000251.3:p.Leu1937Arg
NM_001127180.1:c.5696T>G	NP_001120652.1:p.Leu1899Arg
XM_005274012.2:c.5693T>G	XP_005274069.1:p.Leu1898Arg
XM_006718558.2:c.5801T>G	XP_006718621.1:p.Leu1934Arg
XM_006718559.2:c.5696T>G	XP_006718622.1:p.Leu1899Arg
XM_006718560.2:c.5693T>G	XP_006718623.1:p.Leu1898Arg
XM_006718561.2:c.5696T>G	XP_006718624.1:p.Leu1899Arg
XM_011545044.1:c.5810T>G	XP_011543346.1:p.Leu1937Arg
XM_011545045.1:c.5804T>G	XP_011543347.1:p.Leu1935Arg
XM_011545046.1:c.5777T>G	XP_011543348.1:p.Leu1926Arg
XM_011545047.1:c.5714T>G	XP_011543349.1:p.Leu1905Arg
XM_011545048.1:c.5585T>G	XP_011543350.1:p.Leu1862Arg
XM_011545049.1:c.5573T>G	XP_011543351.1:p.Leu1858Arg
XM_011545050.1:c.5546T>G	XP_011543352.1:p.Leu1849Arg
XM_011545051.1:c.5810T>G	XP_011543353.1:p.Leu1937Arg
XR_949938.1:n.6130T>G
XR_949941.1:n.6130T>G
XM_011545044.2:c.5810T>G	XP_011543346.1:p.Leu1937Arg
XM_011545046.2:c.5900T>G	XP_011543348.2:p.Leu1967Arg
XM_011545050.2:c.5546T>G	XP_011543352.1:p.Leu1849Arg
XM_017017778.1:c.5894T>G	XP_016873267.1:p.Leu1965Arg
XM_017017779.1:c.5891T>G	XP_016873268.1:p.Leu1964Arg
XM_017017780.1:c.5900T>G	XP_016873269.1:p.Leu1967Arg
XM_017017781.1:c.5804T>G	XP_016873270.1:p.Leu1935Arg
XM_017017782.1:c.5786T>G	XP_016873271.1:p.Leu1929Arg
XM_017017783.1:c.5783T>G	XP_016873272.1:p.Leu1928Arg
XM_017017784.1:c.5783T>G	XP_016873273.1:p.Leu1928Arg
XM_017017785.1:c.5663T>G	XP_016873274.1:p.Leu1888Arg
XM_017017786.1:c.5900T>G	XP_016873275.1:p.Leu1967Arg
XM_017017788.1:c.5786T>G	XP_016873277.1:p.Leu1929Arg
XR_001747885.1:n.5915T>G
XR_001747886.1:n.5830T>G
XR_001747887.1:n.5901T>G
NM_000260.4:c.5810T>G MANE Select	NP_000251.3:p.Leu1937Arg
NM_001127180.2:c.5696T>G	NP_001120652.1:p.Leu1899Arg
NM_001369365.1:c.5663T>G	NP_001356294.1:p.Leu1888Arg