Canonical Allele Identifier: CA381936239

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211311C>G , CM000673.2:g.77211311C>G	GRCh38
NC_000011.9:g.76922356C>G , CM000673.1:g.76922356C>G	GRCh37
NC_000011.8:g.76600004C>G	NCBI36
NG_009086.1:g.88047C>G
NG_009086.2:g.88066C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6211C>G MANE Select	ENSP00000386331.3:p.Gln2071Glu
ENST00000670577.1:c.4012C>G
ENST00000409619.6:c.6064C>G	ENSP00000386635.2:p.Gln2022Glu
ENST00000409709.7:c.6211C>G	ENSP00000386331.3:p.Gln2071Glu
ENST00000458169.2:c.3637C>G	ENSP00000417017.2:p.Gln1213Glu
ENST00000458637.6:c.6097C>G	ENSP00000392185.2:p.Gln2033Glu
ENST00000481328.7:n.3747C>G
ENST00000526863.2:n.25+400C>G
ENST00000605744.1:n.1678C>G
NM_000260.3:c.6211C>G	NP_000251.3:p.Gln2071Glu
NM_001127180.1:c.6097C>G	NP_001120652.1:p.Gln2033Glu
XM_005274012.2:c.6094C>G	XP_005274069.1:p.Gln2032Glu
XM_006718558.2:c.6202C>G	XP_006718621.1:p.Gln2068Glu
XM_006718559.2:c.6097C>G	XP_006718622.1:p.Gln2033Glu
XM_006718560.2:c.6094C>G	XP_006718623.1:p.Gln2032Glu
XM_006718561.2:c.6097C>G	XP_006718624.1:p.Gln2033Glu
XM_011545044.1:c.6211C>G	XP_011543346.1:p.Gln2071Glu
XM_011545045.1:c.6205C>G	XP_011543347.1:p.Gln2069Glu
XM_011545046.1:c.6178C>G	XP_011543348.1:p.Gln2060Glu
XM_011545047.1:c.6115C>G	XP_011543349.1:p.Gln2039Glu
XM_011545048.1:c.5986C>G	XP_011543350.1:p.Gln1996Glu
XM_011545049.1:c.5974C>G	XP_011543351.1:p.Gln1992Glu
XM_011545050.1:c.5947C>G	XP_011543352.1:p.Gln1983Glu
XM_011545051.1:c.6211C>G	XP_011543353.1:p.Gln2071Glu
XR_949938.1:n.6531C>G
XR_949941.1:n.6505C>G
XM_011545044.2:c.6211C>G	XP_011543346.1:p.Gln2071Glu
XM_011545046.2:c.6301C>G	XP_011543348.2:p.Gln2101Glu
XM_011545050.2:c.5947C>G	XP_011543352.1:p.Gln1983Glu
XM_017017778.1:c.6295C>G	XP_016873267.1:p.Gln2099Glu
XM_017017779.1:c.6292C>G	XP_016873268.1:p.Gln2098Glu
XM_017017780.1:c.6301C>G	XP_016873269.1:p.Gln2101Glu
XM_017017781.1:c.6205C>G	XP_016873270.1:p.Gln2069Glu
XM_017017782.1:c.6187C>G	XP_016873271.1:p.Gln2063Glu
XM_017017783.1:c.6184C>G	XP_016873272.1:p.Gln2062Glu
XM_017017784.1:c.6184C>G	XP_016873273.1:p.Gln2062Glu
XM_017017785.1:c.6064C>G	XP_016873274.1:p.Gln2022Glu
XM_017017786.1:c.6301C>G	XP_016873275.1:p.Gln2101Glu
XM_017017788.1:c.6187C>G	XP_016873277.1:p.Gln2063Glu
XR_001747885.1:n.6290C>G
XR_001747887.1:n.6276C>G
NM_000260.4:c.6211C>G MANE Select	NP_000251.3:p.Gln2071Glu
NM_001127180.2:c.6097C>G	NP_001120652.1:p.Gln2033Glu
NM_001369365.1:c.6064C>G	NP_001356294.1:p.Gln2022Glu