Canonical Allele Identifier: CA381934739

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76919841A>C (hg19) ; chr11:g.77208796A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77208796A>C , CM000673.2:g.77208796A>C	GRCh38
NC_000011.9:g.76919841A>C , CM000673.1:g.76919841A>C	GRCh37
NC_000011.8:g.76597489A>C	NCBI36
NG_009086.1:g.85532A>C
NG_009086.2:g.85551A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6044A>C MANE Select	ENSP00000386331.3:p.Tyr2015Ser
ENST00000670577.1:c.3845A>C
ENST00000409619.6:c.5897A>C	ENSP00000386635.2:p.Tyr1966Ser
ENST00000409709.7:c.6044A>C	ENSP00000386331.3:p.Tyr2015Ser
ENST00000458169.2:c.3470A>C	ENSP00000417017.2:p.Tyr1157Ser
ENST00000458637.6:c.5930A>C	ENSP00000392185.2:p.Tyr1977Ser
ENST00000481328.7:n.3580A>C
ENST00000605744.1:n.958A>C
NM_000260.3:c.6044A>C	NP_000251.3:p.Tyr2015Ser
NM_001127180.1:c.5930A>C	NP_001120652.1:p.Tyr1977Ser
XM_005274012.2:c.5927A>C	XP_005274069.1:p.Tyr1976Ser
XM_006718558.2:c.6035A>C	XP_006718621.1:p.Tyr2012Ser
XM_006718559.2:c.5930A>C	XP_006718622.1:p.Tyr1977Ser
XM_006718560.2:c.5927A>C	XP_006718623.1:p.Tyr1976Ser
XM_006718561.2:c.5930A>C	XP_006718624.1:p.Tyr1977Ser
XM_011545044.1:c.6044A>C	XP_011543346.1:p.Tyr2015Ser
XM_011545045.1:c.6038A>C	XP_011543347.1:p.Tyr2013Ser
XM_011545046.1:c.6011A>C	XP_011543348.1:p.Tyr2004Ser
XM_011545047.1:c.5948A>C	XP_011543349.1:p.Tyr1983Ser
XM_011545048.1:c.5819A>C	XP_011543350.1:p.Tyr1940Ser
XM_011545049.1:c.5807A>C	XP_011543351.1:p.Tyr1936Ser
XM_011545050.1:c.5780A>C	XP_011543352.1:p.Tyr1927Ser
XM_011545051.1:c.6044A>C	XP_011543353.1:p.Tyr2015Ser
XR_949938.1:n.6364A>C
XR_949941.1:n.6338A>C
XM_011545044.2:c.6044A>C	XP_011543346.1:p.Tyr2015Ser
XM_011545046.2:c.6134A>C	XP_011543348.2:p.Tyr2045Ser
XM_011545050.2:c.5780A>C	XP_011543352.1:p.Tyr1927Ser
XM_017017778.1:c.6128A>C	XP_016873267.1:p.Tyr2043Ser
XM_017017779.1:c.6125A>C	XP_016873268.1:p.Tyr2042Ser
XM_017017780.1:c.6134A>C	XP_016873269.1:p.Tyr2045Ser
XM_017017781.1:c.6038A>C	XP_016873270.1:p.Tyr2013Ser
XM_017017782.1:c.6020A>C	XP_016873271.1:p.Tyr2007Ser
XM_017017783.1:c.6017A>C	XP_016873272.1:p.Tyr2006Ser
XM_017017784.1:c.6017A>C	XP_016873273.1:p.Tyr2006Ser
XM_017017785.1:c.5897A>C	XP_016873274.1:p.Tyr1966Ser
XM_017017786.1:c.6134A>C	XP_016873275.1:p.Tyr2045Ser
XM_017017788.1:c.6020A>C	XP_016873277.1:p.Tyr2007Ser
XR_001747885.1:n.6123A>C
XR_001747886.1:n.6064A>C
XR_001747887.1:n.6109A>C
NM_000260.4:c.6044A>C MANE Select	NP_000251.3:p.Tyr2015Ser
NM_001127180.2:c.5930A>C	NP_001120652.1:p.Tyr1977Ser
NM_001369365.1:c.5897A>C	NP_001356294.1:p.Tyr1966Ser