Canonical Allele Identifier: CA2792788401

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211366_77211367insACAC , CM000673.2:g.77211366_77211367insACAC	GRCh38
NC_000011.9:g.76922411_76922412insACAC , CM000673.1:g.76922411_76922412insACAC	GRCh37
NC_000011.8:g.76600059_76600060insACAC	NCBI36
NG_009086.1:g.88102_88103insACAC
NG_009086.2:g.88121_88122insACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6237+29_6237+30insACAC MANE Select	ENSP00000386331.3:n.6237+29_6237+30insACAC
ENST00000670577.1:c.4038+29_4038+30insACAC
ENST00000409619.6:c.6090+29_6090+30insACAC	ENSP00000386635.2:n.6090+29_6090+30insACAC
ENST00000409709.7:c.6237+29_6237+30insACAC	ENSP00000386331.3:n.6237+29_6237+30insACAC
ENST00000458169.2:c.3663+29_3663+30insACAC	ENSP00000417017.2:n.3663+29_3663+30insACAC
ENST00000458637.6:c.6123+29_6123+30insACAC	ENSP00000392185.2:n.6123+29_6123+30insACAC
ENST00000481328.7:n.3773+29_3773+30insACAC
ENST00000526863.2:n.25+455_25+456insACAC
ENST00000605744.1:n.1704+29_1704+30insACAC
NM_000260.3:c.6237+29_6237+30insACAC	NP_000251.3:n.6237+29_6237+30insACAC
NM_001127180.1:c.6123+29_6123+30insACAC	NP_001120652.1:n.6123+29_6123+30insACAC
XM_005274012.2:c.6120+29_6120+30insACAC	XP_005274069.1:n.6120+29_6120+30insACAC
XM_006718558.2:c.6228+29_6228+30insACAC	XP_006718621.1:n.6228+29_6228+30insACAC
XM_006718559.2:c.6123+29_6123+30insACAC	XP_006718622.1:n.6123+29_6123+30insACAC
XM_006718560.2:c.6120+29_6120+30insACAC	XP_006718623.1:n.6120+29_6120+30insACAC
XM_006718561.2:c.6123+29_6123+30insACAC	XP_006718624.1:n.6123+29_6123+30insACAC
XM_011545044.1:c.6237+29_6237+30insACAC	XP_011543346.1:n.6237+29_6237+30insACAC
XM_011545045.1:c.6231+29_6231+30insACAC	XP_011543347.1:n.6231+29_6231+30insACAC
XM_011545046.1:c.6204+29_6204+30insACAC	XP_011543348.1:n.6204+29_6204+30insACAC
XM_011545047.1:c.6141+29_6141+30insACAC	XP_011543349.1:n.6141+29_6141+30insACAC
XM_011545048.1:c.6012+29_6012+30insACAC	XP_011543350.1:n.6012+29_6012+30insACAC
XM_011545049.1:c.6000+29_6000+30insACAC	XP_011543351.1:n.6000+29_6000+30insACAC
XM_011545050.1:c.5973+29_5973+30insACAC	XP_011543352.1:n.5973+29_5973+30insACAC
XM_011545051.1:c.6237+29_6237+30insACAC	XP_011543353.1:n.6237+29_6237+30insACAC
XR_949938.1:n.6557+29_6557+30insACAC
XR_949941.1:n.6531+29_6531+30insACAC
XM_011545044.2:c.6237+29_6237+30insACAC	XP_011543346.1:n.6237+29_6237+30insACAC
XM_011545046.2:c.6327+29_6327+30insACAC	XP_011543348.2:n.6327+29_6327+30insACAC
XM_011545050.2:c.5973+29_5973+30insACAC	XP_011543352.1:n.5973+29_5973+30insACAC
XM_017017778.1:c.6321+29_6321+30insACAC	XP_016873267.1:n.6321+29_6321+30insACAC
XM_017017779.1:c.6318+29_6318+30insACAC	XP_016873268.1:n.6318+29_6318+30insACAC
XM_017017780.1:c.6327+29_6327+30insACAC	XP_016873269.1:n.6327+29_6327+30insACAC
XM_017017781.1:c.6231+29_6231+30insACAC	XP_016873270.1:n.6231+29_6231+30insACAC
XM_017017782.1:c.6213+29_6213+30insACAC	XP_016873271.1:n.6213+29_6213+30insACAC
XM_017017783.1:c.6210+29_6210+30insACAC	XP_016873272.1:n.6210+29_6210+30insACAC
XM_017017784.1:c.6210+29_6210+30insACAC	XP_016873273.1:n.6210+29_6210+30insACAC
XM_017017785.1:c.6090+29_6090+30insACAC	XP_016873274.1:n.6090+29_6090+30insACAC
XM_017017786.1:c.6327+29_6327+30insACAC	XP_016873275.1:n.6327+29_6327+30insACAC
XM_017017788.1:c.6213+29_6213+30insACAC	XP_016873277.1:n.6213+29_6213+30insACAC
XR_001747885.1:n.6316+29_6316+30insACAC
XR_001747887.1:n.6302+29_6302+30insACAC
NM_000260.4:c.6237+29_6237+30insACAC MANE Select	NP_000251.3:n.6237+29_6237+30insACAC
NM_001127180.2:c.6123+29_6123+30insACAC	NP_001120652.1:n.6123+29_6123+30insACAC
NM_001369365.1:c.6090+29_6090+30insACAC	NP_001356294.1:n.6090+29_6090+30insACAC