Canonical Allele Identifier: CA1984122861

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77199752A= , CM000673.2:g.77199752A=	GRCh38
NC_000011.9:g.76910797A= , CM000673.1:g.76910797A=	GRCh37
NC_000011.8:g.76588445A=	NCBI36
NG_009086.1:g.76488A=
NG_009086.2:g.76507A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.4786A= MANE Select	ENSP00000386331.3:p.Thr1596=
ENST00000670577.1:c.2627A=
ENST00000409619.6:c.4639A=	ENSP00000386635.2:p.Thr1547=
ENST00000409709.7:c.4786A=	ENSP00000386331.3:p.Thr1596=
ENST00000458169.2:c.2215A=	ENSP00000417017.2:p.Thr739=
ENST00000458637.6:c.4672A=	ENSP00000392185.2:p.Thr1558=
ENST00000481328.7:n.2325A=
NM_000260.3:c.4786A=	NP_000251.3:p.Thr1596=
NM_001127180.1:c.4672A=	NP_001120652.1:p.Thr1558=
XM_005274012.2:c.4672A=	XP_005274069.1:p.Thr1558=
XM_006718558.2:c.4780A=	XP_006718621.1:p.Thr1594=
XM_006718559.2:c.4672A=	XP_006718622.1:p.Thr1558=
XM_006718560.2:c.4672A=	XP_006718623.1:p.Thr1558=
XM_006718561.2:c.4672A=	XP_006718624.1:p.Thr1558=
XM_011545044.1:c.4786A=	XP_011543346.1:p.Thr1596=
XM_011545045.1:c.4780A=	XP_011543347.1:p.Thr1594=
XM_011545046.1:c.4753A=	XP_011543348.1:p.Thr1585=
XM_011545047.1:c.4690A=	XP_011543349.1:p.Thr1564=
XM_011545048.1:c.4561A=	XP_011543350.1:p.Thr1521=
XM_011545049.1:c.4549A=	XP_011543351.1:p.Thr1517=
XM_011545050.1:c.4522A=	XP_011543352.1:p.Thr1508=
XM_011545051.1:c.4786A=	XP_011543353.1:p.Thr1596=
XM_011545052.1:c.4786A=	XP_011543354.1:p.Thr1596=
XR_949938.1:n.5106A=
XR_949941.1:n.5106A=
XR_949942.1:n.5108A=
XM_011545044.2:c.4786A=	XP_011543346.1:p.Thr1596=
XM_011545046.2:c.4876A=	XP_011543348.2:p.Thr1626=
XM_011545050.2:c.4522A=	XP_011543352.1:p.Thr1508=
XM_017017778.1:c.4870A=	XP_016873267.1:p.Thr1624=
XM_017017779.1:c.4870A=	XP_016873268.1:p.Thr1624=
XM_017017780.1:c.4876A=	XP_016873269.1:p.Thr1626=
XM_017017781.1:c.4780A=	XP_016873270.1:p.Thr1594=
XM_017017782.1:c.4762A=	XP_016873271.1:p.Thr1588=
XM_017017783.1:c.4762A=	XP_016873272.1:p.Thr1588=
XM_017017784.1:c.4762A=	XP_016873273.1:p.Thr1588=
XM_017017785.1:c.4639A=	XP_016873274.1:p.Thr1547=
XM_017017786.1:c.4876A=	XP_016873275.1:p.Thr1626=
XM_017017788.1:c.4762A=	XP_016873277.1:p.Thr1588=
XR_001747885.1:n.4891A=
XR_001747886.1:n.4891A=
XR_001747887.1:n.4891A=
XR_001747888.1:n.4891A=
NM_000260.4:c.4786A= MANE Select	NP_000251.3:p.Thr1596=
NM_001127180.2:c.4672A=	NP_001120652.1:p.Thr1558=
NM_001369365.1:c.4639A=	NP_001356294.1:p.Thr1547=