Canonical Allele Identifier: CA2615263300

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77211341-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211341A>G , CM000673.2:g.77211341A>G	GRCh38
NC_000011.9:g.76922386A>G , CM000673.1:g.76922386A>G	GRCh37
NC_000011.8:g.76600034A>G	NCBI36
NG_009086.1:g.88077A>G
NG_009086.2:g.88096A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6237+4A>G MANE Select	ENSP00000386331.3:n.6237+4A>G
ENST00000670577.1:c.4038+4A>G
ENST00000409619.6:c.6090+4A>G	ENSP00000386635.2:n.6090+4A>G
ENST00000409709.7:c.6237+4A>G	ENSP00000386331.3:n.6237+4A>G
ENST00000458169.2:c.3663+4A>G	ENSP00000417017.2:n.3663+4A>G
ENST00000458637.6:c.6123+4A>G	ENSP00000392185.2:n.6123+4A>G
ENST00000481328.7:n.3773+4A>G
ENST00000526863.2:n.25+430A>G
ENST00000605744.1:n.1704+4A>G
NM_000260.3:c.6237+4A>G	NP_000251.3:n.6237+4A>G
NM_001127180.1:c.6123+4A>G	NP_001120652.1:n.6123+4A>G
XM_005274012.2:c.6120+4A>G	XP_005274069.1:n.6120+4A>G
XM_006718558.2:c.6228+4A>G	XP_006718621.1:n.6228+4A>G
XM_006718559.2:c.6123+4A>G	XP_006718622.1:n.6123+4A>G
XM_006718560.2:c.6120+4A>G	XP_006718623.1:n.6120+4A>G
XM_006718561.2:c.6123+4A>G	XP_006718624.1:n.6123+4A>G
XM_011545044.1:c.6237+4A>G	XP_011543346.1:n.6237+4A>G
XM_011545045.1:c.6231+4A>G	XP_011543347.1:n.6231+4A>G
XM_011545046.1:c.6204+4A>G	XP_011543348.1:n.6204+4A>G
XM_011545047.1:c.6141+4A>G	XP_011543349.1:n.6141+4A>G
XM_011545048.1:c.6012+4A>G	XP_011543350.1:n.6012+4A>G
XM_011545049.1:c.6000+4A>G	XP_011543351.1:n.6000+4A>G
XM_011545050.1:c.5973+4A>G	XP_011543352.1:n.5973+4A>G
XM_011545051.1:c.6237+4A>G	XP_011543353.1:n.6237+4A>G
XR_949938.1:n.6557+4A>G
XR_949941.1:n.6531+4A>G
XM_011545044.2:c.6237+4A>G	XP_011543346.1:n.6237+4A>G
XM_011545046.2:c.6327+4A>G	XP_011543348.2:n.6327+4A>G
XM_011545050.2:c.5973+4A>G	XP_011543352.1:n.5973+4A>G
XM_017017778.1:c.6321+4A>G	XP_016873267.1:n.6321+4A>G
XM_017017779.1:c.6318+4A>G	XP_016873268.1:n.6318+4A>G
XM_017017780.1:c.6327+4A>G	XP_016873269.1:n.6327+4A>G
XM_017017781.1:c.6231+4A>G	XP_016873270.1:n.6231+4A>G
XM_017017782.1:c.6213+4A>G	XP_016873271.1:n.6213+4A>G
XM_017017783.1:c.6210+4A>G	XP_016873272.1:n.6210+4A>G
XM_017017784.1:c.6210+4A>G	XP_016873273.1:n.6210+4A>G
XM_017017785.1:c.6090+4A>G	XP_016873274.1:n.6090+4A>G
XM_017017786.1:c.6327+4A>G	XP_016873275.1:n.6327+4A>G
XM_017017788.1:c.6213+4A>G	XP_016873277.1:n.6213+4A>G
XR_001747885.1:n.6316+4A>G
XR_001747887.1:n.6302+4A>G
NM_000260.4:c.6237+4A>G MANE Select	NP_000251.3:n.6237+4A>G
NM_001127180.2:c.6123+4A>G	NP_001120652.1:n.6123+4A>G
NM_001369365.1:c.6090+4A>G	NP_001356294.1:n.6090+4A>G