Canonical Allele Identifier: CA381953885

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76918350C>A (hg19) ; chr11:g.77207305C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207305C>A , CM000673.2:g.77207305C>A	GRCh38
NC_000011.9:g.76918350C>A , CM000673.1:g.76918350C>A	GRCh37
NC_000011.8:g.76595998C>A	NCBI36
NG_009086.1:g.84041C>A
NG_009086.2:g.84060C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5759C>A MANE Select	ENSP00000386331.3:p.Ser1920Tyr
ENST00000670577.1:c.3586C>A
ENST00000409619.6:c.5612C>A	ENSP00000386635.2:p.Ser1871Tyr
ENST00000409709.7:c.5759C>A	ENSP00000386331.3:p.Ser1920Tyr
ENST00000458169.2:c.3185C>A	ENSP00000417017.2:p.Ser1062Tyr
ENST00000458637.6:c.5645C>A	ENSP00000392185.2:p.Ser1882Tyr
ENST00000481328.7:n.3295C>A
ENST00000605744.1:n.673C>A
NM_000260.3:c.5759C>A	NP_000251.3:p.Ser1920Tyr
NM_001127180.1:c.5645C>A	NP_001120652.1:p.Ser1882Tyr
XM_005274012.2:c.5642C>A	XP_005274069.1:p.Ser1881Tyr
XM_006718558.2:c.5750C>A	XP_006718621.1:p.Ser1917Tyr
XM_006718559.2:c.5645C>A	XP_006718622.1:p.Ser1882Tyr
XM_006718560.2:c.5642C>A	XP_006718623.1:p.Ser1881Tyr
XM_006718561.2:c.5645C>A	XP_006718624.1:p.Ser1882Tyr
XM_011545044.1:c.5759C>A	XP_011543346.1:p.Ser1920Tyr
XM_011545045.1:c.5753C>A	XP_011543347.1:p.Ser1918Tyr
XM_011545046.1:c.5726C>A	XP_011543348.1:p.Ser1909Tyr
XM_011545047.1:c.5663C>A	XP_011543349.1:p.Ser1888Tyr
XM_011545048.1:c.5534C>A	XP_011543350.1:p.Ser1845Tyr
XM_011545049.1:c.5522C>A	XP_011543351.1:p.Ser1841Tyr
XM_011545050.1:c.5495C>A	XP_011543352.1:p.Ser1832Tyr
XM_011545051.1:c.5759C>A	XP_011543353.1:p.Ser1920Tyr
XR_949938.1:n.6079C>A
XR_949941.1:n.6079C>A
XM_011545044.2:c.5759C>A	XP_011543346.1:p.Ser1920Tyr
XM_011545046.2:c.5849C>A	XP_011543348.2:p.Ser1950Tyr
XM_011545050.2:c.5495C>A	XP_011543352.1:p.Ser1832Tyr
XM_017017778.1:c.5843C>A	XP_016873267.1:p.Ser1948Tyr
XM_017017779.1:c.5840C>A	XP_016873268.1:p.Ser1947Tyr
XM_017017780.1:c.5849C>A	XP_016873269.1:p.Ser1950Tyr
XM_017017781.1:c.5753C>A	XP_016873270.1:p.Ser1918Tyr
XM_017017782.1:c.5735C>A	XP_016873271.1:p.Ser1912Tyr
XM_017017783.1:c.5732C>A	XP_016873272.1:p.Ser1911Tyr
XM_017017784.1:c.5732C>A	XP_016873273.1:p.Ser1911Tyr
XM_017017785.1:c.5612C>A	XP_016873274.1:p.Ser1871Tyr
XM_017017786.1:c.5849C>A	XP_016873275.1:p.Ser1950Tyr
XM_017017788.1:c.5735C>A	XP_016873277.1:p.Ser1912Tyr
XR_001747885.1:n.5864C>A
XR_001747886.1:n.5779C>A
XR_001747887.1:n.5850C>A
NM_000260.4:c.5759C>A MANE Select	NP_000251.3:p.Ser1920Tyr
NM_001127180.2:c.5645C>A	NP_001120652.1:p.Ser1882Tyr
NM_001369365.1:c.5612C>A	NP_001356294.1:p.Ser1871Tyr