Canonical Allele Identifier: CA381953990

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76918374G>T (hg19) ; chr11:g.77207329G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207329G>T , CM000673.2:g.77207329G>T	GRCh38
NC_000011.9:g.76918374G>T , CM000673.1:g.76918374G>T	GRCh37
NC_000011.8:g.76596022G>T	NCBI36
NG_009086.1:g.84065G>T
NG_009086.2:g.84084G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5783G>T MANE Select	ENSP00000386331.3:p.Cys1928Phe
ENST00000670577.1:c.3610G>T
ENST00000409619.6:c.5636G>T	ENSP00000386635.2:p.Cys1879Phe
ENST00000409709.7:c.5783G>T	ENSP00000386331.3:p.Cys1928Phe
ENST00000458169.2:c.3209G>T	ENSP00000417017.2:p.Cys1070Phe
ENST00000458637.6:c.5669G>T	ENSP00000392185.2:p.Cys1890Phe
ENST00000481328.7:n.3319G>T
ENST00000605744.1:n.697G>T
NM_000260.3:c.5783G>T	NP_000251.3:p.Cys1928Phe
NM_001127180.1:c.5669G>T	NP_001120652.1:p.Cys1890Phe
XM_005274012.2:c.5666G>T	XP_005274069.1:p.Cys1889Phe
XM_006718558.2:c.5774G>T	XP_006718621.1:p.Cys1925Phe
XM_006718559.2:c.5669G>T	XP_006718622.1:p.Cys1890Phe
XM_006718560.2:c.5666G>T	XP_006718623.1:p.Cys1889Phe
XM_006718561.2:c.5669G>T	XP_006718624.1:p.Cys1890Phe
XM_011545044.1:c.5783G>T	XP_011543346.1:p.Cys1928Phe
XM_011545045.1:c.5777G>T	XP_011543347.1:p.Cys1926Phe
XM_011545046.1:c.5750G>T	XP_011543348.1:p.Cys1917Phe
XM_011545047.1:c.5687G>T	XP_011543349.1:p.Cys1896Phe
XM_011545048.1:c.5558G>T	XP_011543350.1:p.Cys1853Phe
XM_011545049.1:c.5546G>T	XP_011543351.1:p.Cys1849Phe
XM_011545050.1:c.5519G>T	XP_011543352.1:p.Cys1840Phe
XM_011545051.1:c.5783G>T	XP_011543353.1:p.Cys1928Phe
XR_949938.1:n.6103G>T
XR_949941.1:n.6103G>T
XM_011545044.2:c.5783G>T	XP_011543346.1:p.Cys1928Phe
XM_011545046.2:c.5873G>T	XP_011543348.2:p.Cys1958Phe
XM_011545050.2:c.5519G>T	XP_011543352.1:p.Cys1840Phe
XM_017017778.1:c.5867G>T	XP_016873267.1:p.Cys1956Phe
XM_017017779.1:c.5864G>T	XP_016873268.1:p.Cys1955Phe
XM_017017780.1:c.5873G>T	XP_016873269.1:p.Cys1958Phe
XM_017017781.1:c.5777G>T	XP_016873270.1:p.Cys1926Phe
XM_017017782.1:c.5759G>T	XP_016873271.1:p.Cys1920Phe
XM_017017783.1:c.5756G>T	XP_016873272.1:p.Cys1919Phe
XM_017017784.1:c.5756G>T	XP_016873273.1:p.Cys1919Phe
XM_017017785.1:c.5636G>T	XP_016873274.1:p.Cys1879Phe
XM_017017786.1:c.5873G>T	XP_016873275.1:p.Cys1958Phe
XM_017017788.1:c.5759G>T	XP_016873277.1:p.Cys1920Phe
XR_001747885.1:n.5888G>T
XR_001747886.1:n.5803G>T
XR_001747887.1:n.5874G>T
NM_000260.4:c.5783G>T MANE Select	NP_000251.3:p.Cys1928Phe
NM_001127180.2:c.5669G>T	NP_001120652.1:p.Cys1890Phe
NM_001369365.1:c.5636G>T	NP_001356294.1:p.Cys1879Phe