Canonical Allele Identifier: CA2574932067

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214786T>A , CM000673.2:g.77214786T>A	GRCh38
NC_000011.9:g.76925831T>A , CM000673.1:g.76925831T>A	GRCh37
NC_000011.8:g.76603479T>A	NCBI36
NG_009086.1:g.91522T>A
NG_009086.2:g.91541T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.*90T>A MANE Select	ENSP00000386331.3:n.*90T>A
ENST00000670577.1:c.4539T>A
ENST00000409619.6:c.*90T>A	ENSP00000386635.2:n.*90T>A
ENST00000409709.7:c.*90T>A	ENSP00000386331.3:n.*90T>A
ENST00000458169.2:c.4164T>A	ENSP00000417017.2:n.4164T>A
ENST00000458637.6:c.*90T>A	ENSP00000392185.2:n.*90T>A
ENST00000481328.7:n.5288T>A
ENST00000605744.1:n.2252T>A
NM_000260.3:c.*90T>A	NP_000251.3:n.*90T>A
NM_001127180.1:c.*90T>A	NP_001120652.1:n.*90T>A
XM_005274012.2:c.*90T>A	XP_005274069.1:n.*90T>A
XM_006718561.2:c.*90T>A	XP_006718624.1:n.*90T>A
XR_949941.1:n.7032T>A
XM_017017780.1:c.*90T>A	XP_016873269.1:n.*90T>A
XM_017017784.1:c.*90T>A	XP_016873273.1:n.*90T>A
XM_017017788.1:c.*90T>A	XP_016873277.1:n.*90T>A
XR_001747885.1:n.6817T>A
XR_001747887.1:n.6803T>A
NM_000260.4:c.*90T>A MANE Select	NP_000251.3:n.*90T>A
NM_001127180.2:c.*90T>A	NP_001120652.1:n.*90T>A
NM_001369365.1:c.*90T>A	NP_001356294.1:n.*90T>A