Canonical Allele Identifier: CA2574932070

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214792A>G , CM000673.2:g.77214792A>G	GRCh38
NC_000011.9:g.76925837A>G , CM000673.1:g.76925837A>G	GRCh37
NC_000011.8:g.76603485A>G	NCBI36
NG_009086.1:g.91528A>G
NG_009086.2:g.91547A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.*96A>G MANE Select	ENSP00000386331.3:n.*96A>G
ENST00000670577.1:c.4545A>G
ENST00000409619.6:c.*96A>G	ENSP00000386635.2:n.*96A>G
ENST00000409709.7:c.*96A>G	ENSP00000386331.3:n.*96A>G
ENST00000458169.2:c.4170A>G	ENSP00000417017.2:n.4170A>G
ENST00000458637.6:c.*96A>G	ENSP00000392185.2:n.*96A>G
ENST00000481328.7:n.5294A>G
ENST00000605744.1:n.2258A>G
NM_000260.3:c.*96A>G	NP_000251.3:n.*96A>G
NM_001127180.1:c.*96A>G	NP_001120652.1:n.*96A>G
XM_005274012.2:c.*96A>G	XP_005274069.1:n.*96A>G
XM_006718561.2:c.*96A>G	XP_006718624.1:n.*96A>G
XR_949941.1:n.7038A>G
XM_017017780.1:c.*96A>G	XP_016873269.1:n.*96A>G
XM_017017784.1:c.*96A>G	XP_016873273.1:n.*96A>G
XM_017017788.1:c.*96A>G	XP_016873277.1:n.*96A>G
XR_001747885.1:n.6823A>G
XR_001747887.1:n.6809A>G
NM_000260.4:c.*96A>G MANE Select	NP_000251.3:n.*96A>G
NM_001127180.2:c.*96A>G	NP_001120652.1:n.*96A>G
NM_001369365.1:c.*96A>G	NP_001356294.1:n.*96A>G