Canonical Allele Identifier: CA381936457

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211835C>A , CM000673.2:g.77211835C>A	GRCh38
NC_000011.9:g.76922880C>A , CM000673.1:g.76922880C>A	GRCh37
NC_000011.8:g.76600528C>A	NCBI36
NG_009086.1:g.88571C>A
NG_009086.2:g.88590C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000260.4:c.6252C>A MANE Select	NP_000251.3:p.Tyr2084Ter
ENST00000409709.9:c.6252C>A MANE Select	ENSP00000386331.3:p.Tyr2084Ter
NM_000260.3:c.6252C>A	NP_000251.3:p.Tyr2084Ter
NM_001127180.1:c.6138C>A	NP_001120652.1:p.Tyr2046Ter
NM_001127180.2:c.6138C>A	NP_001120652.1:p.Tyr2046Ter
NM_001369365.1:c.6105C>A	NP_001356294.1:p.Tyr2035Ter
ENST00000409619.6:c.6105C>A	ENSP00000386635.2:p.Tyr2035Ter
ENST00000409709.7:c.6252C>A	ENSP00000386331.3:p.Tyr2084Ter
ENST00000458169.2:c.3678C>A	ENSP00000417017.2:p.Tyr1226Ter
ENST00000458637.6:c.6138C>A	ENSP00000392185.2:p.Tyr2046Ter
ENST00000481328.7:n.3788C>A
ENST00000526863.2:n.26-710C>A
ENST00000605744.1:n.1719C>A
ENST00000670577.1:c.4053C>A
XM_005274012.2:c.6135C>A	XP_005274069.1:p.Tyr2045Ter
XM_006718558.2:c.6243C>A	XP_006718621.1:p.Tyr2081Ter
XM_006718559.2:c.6138C>A	XP_006718622.1:p.Tyr2046Ter
XM_006718560.2:c.6135C>A	XP_006718623.1:p.Tyr2045Ter
XM_006718561.2:c.6138C>A	XP_006718624.1:p.Tyr2046Ter
XM_011545044.1:c.6252C>A	XP_011543346.1:p.Tyr2084Ter
XM_011545044.2:c.6252C>A	XP_011543346.1:p.Tyr2084Ter
XM_011545045.1:c.6246C>A	XP_011543347.1:p.Tyr2082Ter
XM_011545046.1:c.6219C>A	XP_011543348.1:p.Tyr2073Ter
XM_011545046.2:c.6342C>A	XP_011543348.2:p.Tyr2114Ter
XM_011545047.1:c.6156C>A	XP_011543349.1:p.Tyr2052Ter
XM_011545048.1:c.6027C>A	XP_011543350.1:p.Tyr2009Ter
XM_011545049.1:c.6015C>A	XP_011543351.1:p.Tyr2005Ter
XM_011545050.1:c.5988C>A	XP_011543352.1:p.Tyr1996Ter
XM_011545050.2:c.5988C>A	XP_011543352.1:p.Tyr1996Ter
XM_011545051.1:c.6252C>A	XP_011543353.1:p.Tyr2084Ter
XM_017017778.1:c.6336C>A	XP_016873267.1:p.Tyr2112Ter
XM_017017779.1:c.6333C>A	XP_016873268.1:p.Tyr2111Ter
XM_017017780.1:c.6342C>A	XP_016873269.1:p.Tyr2114Ter
XM_017017781.1:c.6246C>A	XP_016873270.1:p.Tyr2082Ter
XM_017017782.1:c.6228C>A	XP_016873271.1:p.Tyr2076Ter
XM_017017783.1:c.6225C>A	XP_016873272.1:p.Tyr2075Ter
XM_017017784.1:c.6225C>A	XP_016873273.1:p.Tyr2075Ter
XM_017017785.1:c.6105C>A	XP_016873274.1:p.Tyr2035Ter
XM_017017786.1:c.6342C>A	XP_016873275.1:p.Tyr2114Ter
XM_017017788.1:c.6228C>A	XP_016873277.1:p.Tyr2076Ter
XR_001747885.1:n.6331C>A
XR_001747887.1:n.6317C>A
XR_949938.1:n.6572C>A
XR_949941.1:n.6546C>A