Canonical Allele Identifier: CA381954092

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76918415G>C (hg19) ; chr11:g.77207370G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207370G>C , CM000673.2:g.77207370G>C	GRCh38
NC_000011.9:g.76918415G>C , CM000673.1:g.76918415G>C	GRCh37
NC_000011.8:g.76596063G>C	NCBI36
NG_009086.1:g.84106G>C
NG_009086.2:g.84125G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5824G>C MANE Select	ENSP00000386331.3:p.Gly1942Arg
ENST00000670577.1:c.3651G>C
ENST00000409619.6:c.5677G>C	ENSP00000386635.2:p.Gly1893Arg
ENST00000409709.7:c.5824G>C	ENSP00000386331.3:p.Gly1942Arg
ENST00000458169.2:c.3250G>C	ENSP00000417017.2:p.Gly1084Arg
ENST00000458637.6:c.5710G>C	ENSP00000392185.2:p.Gly1904Arg
ENST00000481328.7:n.3360G>C
ENST00000605744.1:n.738G>C
NM_000260.3:c.5824G>C	NP_000251.3:p.Gly1942Arg
NM_001127180.1:c.5710G>C	NP_001120652.1:p.Gly1904Arg
XM_005274012.2:c.5707G>C	XP_005274069.1:p.Gly1903Arg
XM_006718558.2:c.5815G>C	XP_006718621.1:p.Gly1939Arg
XM_006718559.2:c.5710G>C	XP_006718622.1:p.Gly1904Arg
XM_006718560.2:c.5707G>C	XP_006718623.1:p.Gly1903Arg
XM_006718561.2:c.5710G>C	XP_006718624.1:p.Gly1904Arg
XM_011545044.1:c.5824G>C	XP_011543346.1:p.Gly1942Arg
XM_011545045.1:c.5818G>C	XP_011543347.1:p.Gly1940Arg
XM_011545046.1:c.5791G>C	XP_011543348.1:p.Gly1931Arg
XM_011545047.1:c.5728G>C	XP_011543349.1:p.Gly1910Arg
XM_011545048.1:c.5599G>C	XP_011543350.1:p.Gly1867Arg
XM_011545049.1:c.5587G>C	XP_011543351.1:p.Gly1863Arg
XM_011545050.1:c.5560G>C	XP_011543352.1:p.Gly1854Arg
XM_011545051.1:c.5824G>C	XP_011543353.1:p.Gly1942Arg
XR_949938.1:n.6144G>C
XR_949941.1:n.6144G>C
XM_011545044.2:c.5824G>C	XP_011543346.1:p.Gly1942Arg
XM_011545046.2:c.5914G>C	XP_011543348.2:p.Gly1972Arg
XM_011545050.2:c.5560G>C	XP_011543352.1:p.Gly1854Arg
XM_017017778.1:c.5908G>C	XP_016873267.1:p.Gly1970Arg
XM_017017779.1:c.5905G>C	XP_016873268.1:p.Gly1969Arg
XM_017017780.1:c.5914G>C	XP_016873269.1:p.Gly1972Arg
XM_017017781.1:c.5818G>C	XP_016873270.1:p.Gly1940Arg
XM_017017782.1:c.5800G>C	XP_016873271.1:p.Gly1934Arg
XM_017017783.1:c.5797G>C	XP_016873272.1:p.Gly1933Arg
XM_017017784.1:c.5797G>C	XP_016873273.1:p.Gly1933Arg
XM_017017785.1:c.5677G>C	XP_016873274.1:p.Gly1893Arg
XM_017017786.1:c.5914G>C	XP_016873275.1:p.Gly1972Arg
XM_017017788.1:c.5800G>C	XP_016873277.1:p.Gly1934Arg
XR_001747885.1:n.5929G>C
XR_001747886.1:n.5844G>C
XR_001747887.1:n.5915G>C
NM_000260.4:c.5824G>C MANE Select	NP_000251.3:p.Gly1942Arg
NM_001127180.2:c.5710G>C	NP_001120652.1:p.Gly1904Arg
NM_001369365.1:c.5677G>C	NP_001356294.1:p.Gly1893Arg