Canonical Allele Identifier: CA381935825

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76922269T>G (hg19) ; chr11:g.77211224T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211224T>G , CM000673.2:g.77211224T>G	GRCh38
NC_000011.9:g.76922269T>G , CM000673.1:g.76922269T>G	GRCh37
NC_000011.8:g.76599917T>G	NCBI36
NG_009086.1:g.87960T>G
NG_009086.2:g.87979T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.6124T>G MANE Select	ENSP00000386331.3:p.Tyr2042Asp
ENST00000670577.1:c.3925T>G
ENST00000409619.6:c.5977T>G	ENSP00000386635.2:p.Tyr1993Asp
ENST00000409709.7:c.6124T>G	ENSP00000386331.3:p.Tyr2042Asp
ENST00000458169.2:c.3550T>G	ENSP00000417017.2:p.Tyr1184Asp
ENST00000458637.6:c.6010T>G	ENSP00000392185.2:p.Tyr2004Asp
ENST00000481328.7:n.3660T>G
ENST00000526863.2:n.25+313T>G
ENST00000605744.1:n.1591T>G
NM_000260.3:c.6124T>G	NP_000251.3:p.Tyr2042Asp
NM_001127180.1:c.6010T>G	NP_001120652.1:p.Tyr2004Asp
XM_005274012.2:c.6007T>G	XP_005274069.1:p.Tyr2003Asp
XM_006718558.2:c.6115T>G	XP_006718621.1:p.Tyr2039Asp
XM_006718559.2:c.6010T>G	XP_006718622.1:p.Tyr2004Asp
XM_006718560.2:c.6007T>G	XP_006718623.1:p.Tyr2003Asp
XM_006718561.2:c.6010T>G	XP_006718624.1:p.Tyr2004Asp
XM_011545044.1:c.6124T>G	XP_011543346.1:p.Tyr2042Asp
XM_011545045.1:c.6118T>G	XP_011543347.1:p.Tyr2040Asp
XM_011545046.1:c.6091T>G	XP_011543348.1:p.Tyr2031Asp
XM_011545047.1:c.6028T>G	XP_011543349.1:p.Tyr2010Asp
XM_011545048.1:c.5899T>G	XP_011543350.1:p.Tyr1967Asp
XM_011545049.1:c.5887T>G	XP_011543351.1:p.Tyr1963Asp
XM_011545050.1:c.5860T>G	XP_011543352.1:p.Tyr1954Asp
XM_011545051.1:c.6124T>G	XP_011543353.1:p.Tyr2042Asp
XR_949938.1:n.6444T>G
XR_949941.1:n.6418T>G
XM_011545044.2:c.6124T>G	XP_011543346.1:p.Tyr2042Asp
XM_011545046.2:c.6214T>G	XP_011543348.2:p.Tyr2072Asp
XM_011545050.2:c.5860T>G	XP_011543352.1:p.Tyr1954Asp
XM_017017778.1:c.6208T>G	XP_016873267.1:p.Tyr2070Asp
XM_017017779.1:c.6205T>G	XP_016873268.1:p.Tyr2069Asp
XM_017017780.1:c.6214T>G	XP_016873269.1:p.Tyr2072Asp
XM_017017781.1:c.6118T>G	XP_016873270.1:p.Tyr2040Asp
XM_017017782.1:c.6100T>G	XP_016873271.1:p.Tyr2034Asp
XM_017017783.1:c.6097T>G	XP_016873272.1:p.Tyr2033Asp
XM_017017784.1:c.6097T>G	XP_016873273.1:p.Tyr2033Asp
XM_017017785.1:c.5977T>G	XP_016873274.1:p.Tyr1993Asp
XM_017017786.1:c.6214T>G	XP_016873275.1:p.Tyr2072Asp
XM_017017788.1:c.6100T>G	XP_016873277.1:p.Tyr2034Asp
XR_001747885.1:n.6203T>G
XR_001747886.1:n.6144T>G
XR_001747887.1:n.6189T>G
NM_000260.4:c.6124T>G MANE Select	NP_000251.3:p.Tyr2042Asp
NM_001127180.2:c.6010T>G	NP_001120652.1:p.Tyr2004Asp
NM_001369365.1:c.5977T>G	NP_001356294.1:p.Tyr1993Asp