Canonical Allele Identifier: CA475797291

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76918348G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207303G>A , CM000673.2:g.77207303G>A	GRCh38
NC_000011.9:g.76918348G>A , CM000673.1:g.76918348G>A	GRCh37
NC_000011.8:g.76595996G>A	NCBI36
NG_009086.1:g.84039G>A
NG_009086.2:g.84058G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5757G>A MANE Select	ENSP00000386331.3:p.Glu1919=
ENST00000670577.1:c.3584G>A
ENST00000409619.6:c.5610G>A	ENSP00000386635.2:p.Glu1870=
ENST00000409709.7:c.5757G>A	ENSP00000386331.3:p.Glu1919=
ENST00000458169.2:c.3183G>A	ENSP00000417017.2:p.Glu1061=
ENST00000458637.6:c.5643G>A	ENSP00000392185.2:p.Glu1881=
ENST00000481328.7:n.3293G>A
ENST00000605744.1:n.671G>A
NM_000260.3:c.5757G>A	NP_000251.3:p.Glu1919=
NM_001127180.1:c.5643G>A	NP_001120652.1:p.Glu1881=
XM_005274012.2:c.5640G>A	XP_005274069.1:p.Glu1880=
XM_006718558.2:c.5748G>A	XP_006718621.1:p.Glu1916=
XM_006718559.2:c.5643G>A	XP_006718622.1:p.Glu1881=
XM_006718560.2:c.5640G>A	XP_006718623.1:p.Glu1880=
XM_006718561.2:c.5643G>A	XP_006718624.1:p.Glu1881=
XM_011545044.1:c.5757G>A	XP_011543346.1:p.Glu1919=
XM_011545045.1:c.5751G>A	XP_011543347.1:p.Glu1917=
XM_011545046.1:c.5724G>A	XP_011543348.1:p.Glu1908=
XM_011545047.1:c.5661G>A	XP_011543349.1:p.Glu1887=
XM_011545048.1:c.5532G>A	XP_011543350.1:p.Glu1844=
XM_011545049.1:c.5520G>A	XP_011543351.1:p.Glu1840=
XM_011545050.1:c.5493G>A	XP_011543352.1:p.Glu1831=
XM_011545051.1:c.5757G>A	XP_011543353.1:p.Glu1919=
XR_949938.1:n.6077G>A
XR_949941.1:n.6077G>A
XM_011545044.2:c.5757G>A	XP_011543346.1:p.Glu1919=
XM_011545046.2:c.5847G>A	XP_011543348.2:p.Glu1949=
XM_011545050.2:c.5493G>A	XP_011543352.1:p.Glu1831=
XM_017017778.1:c.5841G>A	XP_016873267.1:p.Glu1947=
XM_017017779.1:c.5838G>A	XP_016873268.1:p.Glu1946=
XM_017017780.1:c.5847G>A	XP_016873269.1:p.Glu1949=
XM_017017781.1:c.5751G>A	XP_016873270.1:p.Glu1917=
XM_017017782.1:c.5733G>A	XP_016873271.1:p.Glu1911=
XM_017017783.1:c.5730G>A	XP_016873272.1:p.Glu1910=
XM_017017784.1:c.5730G>A	XP_016873273.1:p.Glu1910=
XM_017017785.1:c.5610G>A	XP_016873274.1:p.Glu1870=
XM_017017786.1:c.5847G>A	XP_016873275.1:p.Glu1949=
XM_017017788.1:c.5733G>A	XP_016873277.1:p.Glu1911=
XR_001747885.1:n.5862G>A
XR_001747886.1:n.5777G>A
XR_001747887.1:n.5848G>A
NM_000260.4:c.5757G>A MANE Select	NP_000251.3:p.Glu1919=
NM_001127180.2:c.5643G>A	NP_001120652.1:p.Glu1881=
NM_001369365.1:c.5610G>A	NP_001356294.1:p.Glu1870=