Canonical Allele Identifier: CA2792788414

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211420_77211421insA , CM000673.2:g.77211420_77211421insA	GRCh38
NC_000011.9:g.76922465_76922466insA , CM000673.1:g.76922465_76922466insA	GRCh37
NC_000011.8:g.76600113_76600114insA	NCBI36
NG_009086.1:g.88156_88157insA
NG_009086.2:g.88175_88176insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6237+83_6237+84insA MANE Select	ENSP00000386331.3:n.6237+83_6237+84insA
ENST00000670577.1:c.4038+83_4038+84insA
ENST00000409619.6:c.6090+83_6090+84insA	ENSP00000386635.2:n.6090+83_6090+84insA
ENST00000409709.7:c.6237+83_6237+84insA	ENSP00000386331.3:n.6237+83_6237+84insA
ENST00000458169.2:c.3663+83_3663+84insA	ENSP00000417017.2:n.3663+83_3663+84insA
ENST00000458637.6:c.6123+83_6123+84insA	ENSP00000392185.2:n.6123+83_6123+84insA
ENST00000481328.7:n.3773+83_3773+84insA
ENST00000526863.2:n.25+509_25+510insA
ENST00000605744.1:n.1704+83_1704+84insA
NM_000260.3:c.6237+83_6237+84insA	NP_000251.3:n.6237+83_6237+84insA
NM_001127180.1:c.6123+83_6123+84insA	NP_001120652.1:n.6123+83_6123+84insA
XM_005274012.2:c.6120+83_6120+84insA	XP_005274069.1:n.6120+83_6120+84insA
XM_006718558.2:c.6228+83_6228+84insA	XP_006718621.1:n.6228+83_6228+84insA
XM_006718559.2:c.6123+83_6123+84insA	XP_006718622.1:n.6123+83_6123+84insA
XM_006718560.2:c.6120+83_6120+84insA	XP_006718623.1:n.6120+83_6120+84insA
XM_006718561.2:c.6123+83_6123+84insA	XP_006718624.1:n.6123+83_6123+84insA
XM_011545044.1:c.6237+83_6237+84insA	XP_011543346.1:n.6237+83_6237+84insA
XM_011545045.1:c.6231+83_6231+84insA	XP_011543347.1:n.6231+83_6231+84insA
XM_011545046.1:c.6204+83_6204+84insA	XP_011543348.1:n.6204+83_6204+84insA
XM_011545047.1:c.6141+83_6141+84insA	XP_011543349.1:n.6141+83_6141+84insA
XM_011545048.1:c.6012+83_6012+84insA	XP_011543350.1:n.6012+83_6012+84insA
XM_011545049.1:c.6000+83_6000+84insA	XP_011543351.1:n.6000+83_6000+84insA
XM_011545050.1:c.5973+83_5973+84insA	XP_011543352.1:n.5973+83_5973+84insA
XM_011545051.1:c.6237+83_6237+84insA	XP_011543353.1:n.6237+83_6237+84insA
XR_949938.1:n.6557+83_6557+84insA
XR_949941.1:n.6531+83_6531+84insA
XM_011545044.2:c.6237+83_6237+84insA	XP_011543346.1:n.6237+83_6237+84insA
XM_011545046.2:c.6327+83_6327+84insA	XP_011543348.2:n.6327+83_6327+84insA
XM_011545050.2:c.5973+83_5973+84insA	XP_011543352.1:n.5973+83_5973+84insA
XM_017017778.1:c.6321+83_6321+84insA	XP_016873267.1:n.6321+83_6321+84insA
XM_017017779.1:c.6318+83_6318+84insA	XP_016873268.1:n.6318+83_6318+84insA
XM_017017780.1:c.6327+83_6327+84insA	XP_016873269.1:n.6327+83_6327+84insA
XM_017017781.1:c.6231+83_6231+84insA	XP_016873270.1:n.6231+83_6231+84insA
XM_017017782.1:c.6213+83_6213+84insA	XP_016873271.1:n.6213+83_6213+84insA
XM_017017783.1:c.6210+83_6210+84insA	XP_016873272.1:n.6210+83_6210+84insA
XM_017017784.1:c.6210+83_6210+84insA	XP_016873273.1:n.6210+83_6210+84insA
XM_017017785.1:c.6090+83_6090+84insA	XP_016873274.1:n.6090+83_6090+84insA
XM_017017786.1:c.6327+83_6327+84insA	XP_016873275.1:n.6327+83_6327+84insA
XM_017017788.1:c.6213+83_6213+84insA	XP_016873277.1:n.6213+83_6213+84insA
XR_001747885.1:n.6316+83_6316+84insA
XR_001747887.1:n.6302+83_6302+84insA
NM_000260.4:c.6237+83_6237+84insA MANE Select	NP_000251.3:n.6237+83_6237+84insA
NM_001127180.2:c.6123+83_6123+84insA	NP_001120652.1:n.6123+83_6123+84insA
NM_001369365.1:c.6090+83_6090+84insA	NP_001356294.1:n.6090+83_6090+84insA