Canonical Allele Identifier: CA1984129911

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211318C= , CM000673.2:g.77211318C=	GRCh38
NC_000011.9:g.76922363C= , CM000673.1:g.76922363C=	GRCh37
NC_000011.8:g.76600011C=	NCBI36
NG_009086.1:g.88054C=
NG_009086.2:g.88073C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6218C= MANE Select	ENSP00000386331.3:p.Ser2073=
ENST00000670577.1:c.4019C=
ENST00000409619.6:c.6071C=	ENSP00000386635.2:p.Ser2024=
ENST00000409709.7:c.6218C=	ENSP00000386331.3:p.Ser2073=
ENST00000458169.2:c.3644C=	ENSP00000417017.2:p.Ser1215=
ENST00000458637.6:c.6104C=	ENSP00000392185.2:p.Ser2035=
ENST00000481328.7:n.3754C=
ENST00000526863.2:n.25+407C=
ENST00000605744.1:n.1685C=
NM_000260.3:c.6218C=	NP_000251.3:p.Ser2073=
NM_001127180.1:c.6104C=	NP_001120652.1:p.Ser2035=
XM_005274012.2:c.6101C=	XP_005274069.1:p.Ser2034=
XM_006718558.2:c.6209C=	XP_006718621.1:p.Ser2070=
XM_006718559.2:c.6104C=	XP_006718622.1:p.Ser2035=
XM_006718560.2:c.6101C=	XP_006718623.1:p.Ser2034=
XM_006718561.2:c.6104C=	XP_006718624.1:p.Ser2035=
XM_011545044.1:c.6218C=	XP_011543346.1:p.Ser2073=
XM_011545045.1:c.6212C=	XP_011543347.1:p.Ser2071=
XM_011545046.1:c.6185C=	XP_011543348.1:p.Ser2062=
XM_011545047.1:c.6122C=	XP_011543349.1:p.Ser2041=
XM_011545048.1:c.5993C=	XP_011543350.1:p.Ser1998=
XM_011545049.1:c.5981C=	XP_011543351.1:p.Ser1994=
XM_011545050.1:c.5954C=	XP_011543352.1:p.Ser1985=
XM_011545051.1:c.6218C=	XP_011543353.1:p.Ser2073=
XR_949938.1:n.6538C=
XR_949941.1:n.6512C=
XM_011545044.2:c.6218C=	XP_011543346.1:p.Ser2073=
XM_011545046.2:c.6308C=	XP_011543348.2:p.Ser2103=
XM_011545050.2:c.5954C=	XP_011543352.1:p.Ser1985=
XM_017017778.1:c.6302C=	XP_016873267.1:p.Ser2101=
XM_017017779.1:c.6299C=	XP_016873268.1:p.Ser2100=
XM_017017780.1:c.6308C=	XP_016873269.1:p.Ser2103=
XM_017017781.1:c.6212C=	XP_016873270.1:p.Ser2071=
XM_017017782.1:c.6194C=	XP_016873271.1:p.Ser2065=
XM_017017783.1:c.6191C=	XP_016873272.1:p.Ser2064=
XM_017017784.1:c.6191C=	XP_016873273.1:p.Ser2064=
XM_017017785.1:c.6071C=	XP_016873274.1:p.Ser2024=
XM_017017786.1:c.6308C=	XP_016873275.1:p.Ser2103=
XM_017017788.1:c.6194C=	XP_016873277.1:p.Ser2065=
XR_001747885.1:n.6297C=
XR_001747887.1:n.6283C=
NM_000260.4:c.6218C= MANE Select	NP_000251.3:p.Ser2073=
NM_001127180.2:c.6104C=	NP_001120652.1:p.Ser2035=
NM_001369365.1:c.6071C=	NP_001356294.1:p.Ser2024=