Canonical Allele Identifier: CA2573053571

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77212974del , CM000673.2:g.77212974del	GRCh38
NC_000011.9:g.76924019del , CM000673.1:g.76924019del	GRCh37
NC_000011.8:g.76601667del	NCBI36
NG_009086.1:g.89710del
NG_009086.2:g.89729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6377del MANE Select	ENSP00000386331.3:p.Pro2126LeufsTer5
ENST00000670577.1:c.4178del
ENST00000409619.6:c.6230del	ENSP00000386635.2:p.Pro2077LeufsTer5
ENST00000409709.7:c.6377del	ENSP00000386331.3:p.Pro2126LeufsTer5
ENST00000458169.2:c.3803del	ENSP00000417017.2:p.Pro1268LeufsTer5
ENST00000458637.6:c.6257del	ENSP00000392185.2:p.Pro2086LeufsTer5
ENST00000481328.7:n.4927del
ENST00000481532.1:n.440del
ENST00000526863.2:n.455del
ENST00000605744.1:n.1891del
NM_000260.3:c.6377del	NP_000251.3:p.Pro2126LeufsTer5
NM_001127180.1:c.6257del	NP_001120652.1:p.Pro2086LeufsTer5
XM_005274012.2:c.6260del	XP_005274069.1:p.Pro2087LeufsTer5
XM_006718561.2:c.6263del	XP_006718624.1:p.Pro2088LeufsTer5
XM_011545051.1:c.*49del	XP_011543353.1:n.*49del
XR_949941.1:n.6671del
XM_017017780.1:c.6467del	XP_016873269.1:p.Pro2156LeufsTer5
XM_017017784.1:c.6350del	XP_016873273.1:p.Pro2117LeufsTer5
XM_017017786.1:c.*49del	XP_016873275.1:n.*49del
XM_017017788.1:c.6353del	XP_016873277.1:p.Pro2118LeufsTer5
XR_001747885.1:n.6456del
XR_001747887.1:n.6442del
NM_000260.4:c.6377del MANE Select	NP_000251.3:p.Pro2126LeufsTer5
NM_001127180.2:c.6257del	NP_001120652.1:p.Pro2086LeufsTer5
NM_001369365.1:c.6230del	NP_001356294.1:p.Pro2077LeufsTer5