Canonical Allele Identifier: CA475792066

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76922367T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211322T>A , CM000673.2:g.77211322T>A	GRCh38
NC_000011.9:g.76922367T>A , CM000673.1:g.76922367T>A	GRCh37
NC_000011.8:g.76600015T>A	NCBI36
NG_009086.1:g.88058T>A
NG_009086.2:g.88077T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.6222T>A MANE Select	ENSP00000386331.3:p.Pro2074=
ENST00000670577.1:c.4023T>A
ENST00000409619.6:c.6075T>A	ENSP00000386635.2:p.Pro2025=
ENST00000409709.7:c.6222T>A	ENSP00000386331.3:p.Pro2074=
ENST00000458169.2:c.3648T>A	ENSP00000417017.2:p.Pro1216=
ENST00000458637.6:c.6108T>A	ENSP00000392185.2:p.Pro2036=
ENST00000481328.7:n.3758T>A
ENST00000526863.2:n.25+411T>A
ENST00000605744.1:n.1689T>A
NM_000260.3:c.6222T>A	NP_000251.3:p.Pro2074=
NM_001127180.1:c.6108T>A	NP_001120652.1:p.Pro2036=
XM_005274012.2:c.6105T>A	XP_005274069.1:p.Pro2035=
XM_006718558.2:c.6213T>A	XP_006718621.1:p.Pro2071=
XM_006718559.2:c.6108T>A	XP_006718622.1:p.Pro2036=
XM_006718560.2:c.6105T>A	XP_006718623.1:p.Pro2035=
XM_006718561.2:c.6108T>A	XP_006718624.1:p.Pro2036=
XM_011545044.1:c.6222T>A	XP_011543346.1:p.Pro2074=
XM_011545045.1:c.6216T>A	XP_011543347.1:p.Pro2072=
XM_011545046.1:c.6189T>A	XP_011543348.1:p.Pro2063=
XM_011545047.1:c.6126T>A	XP_011543349.1:p.Pro2042=
XM_011545048.1:c.5997T>A	XP_011543350.1:p.Pro1999=
XM_011545049.1:c.5985T>A	XP_011543351.1:p.Pro1995=
XM_011545050.1:c.5958T>A	XP_011543352.1:p.Pro1986=
XM_011545051.1:c.6222T>A	XP_011543353.1:p.Pro2074=
XR_949938.1:n.6542T>A
XR_949941.1:n.6516T>A
XM_011545044.2:c.6222T>A	XP_011543346.1:p.Pro2074=
XM_011545046.2:c.6312T>A	XP_011543348.2:p.Pro2104=
XM_011545050.2:c.5958T>A	XP_011543352.1:p.Pro1986=
XM_017017778.1:c.6306T>A	XP_016873267.1:p.Pro2102=
XM_017017779.1:c.6303T>A	XP_016873268.1:p.Pro2101=
XM_017017780.1:c.6312T>A	XP_016873269.1:p.Pro2104=
XM_017017781.1:c.6216T>A	XP_016873270.1:p.Pro2072=
XM_017017782.1:c.6198T>A	XP_016873271.1:p.Pro2066=
XM_017017783.1:c.6195T>A	XP_016873272.1:p.Pro2065=
XM_017017784.1:c.6195T>A	XP_016873273.1:p.Pro2065=
XM_017017785.1:c.6075T>A	XP_016873274.1:p.Pro2025=
XM_017017786.1:c.6312T>A	XP_016873275.1:p.Pro2104=
XM_017017788.1:c.6198T>A	XP_016873277.1:p.Pro2066=
XR_001747885.1:n.6301T>A
XR_001747887.1:n.6287T>A
NM_000260.4:c.6222T>A MANE Select	NP_000251.3:p.Pro2074=
NM_001127180.2:c.6108T>A	NP_001120652.1:p.Pro2036=
NM_001369365.1:c.6075T>A	NP_001356294.1:p.Pro2025=