Canonical Allele Identifier: CA381936330

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77211328-C-A
• MyVariant Identifiers: chr11:g.76922373C>A (hg19) ; chr11:g.77211328C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211328C>A , CM000673.2:g.77211328C>A	GRCh38
NC_000011.9:g.76922373C>A , CM000673.1:g.76922373C>A	GRCh37
NC_000011.8:g.76600021C>A	NCBI36
NG_009086.1:g.88064C>A
NG_009086.2:g.88083C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6228C>A MANE Select	ENSP00000386331.3:p.Asp2076Glu
ENST00000670577.1:c.4029C>A
ENST00000409619.6:c.6081C>A	ENSP00000386635.2:p.Asp2027Glu
ENST00000409709.7:c.6228C>A	ENSP00000386331.3:p.Asp2076Glu
ENST00000458169.2:c.3654C>A	ENSP00000417017.2:p.Asp1218Glu
ENST00000458637.6:c.6114C>A	ENSP00000392185.2:p.Asp2038Glu
ENST00000481328.7:n.3764C>A
ENST00000526863.2:n.25+417C>A
ENST00000605744.1:n.1695C>A
NM_000260.3:c.6228C>A	NP_000251.3:p.Asp2076Glu
NM_001127180.1:c.6114C>A	NP_001120652.1:p.Asp2038Glu
XM_005274012.2:c.6111C>A	XP_005274069.1:p.Asp2037Glu
XM_006718558.2:c.6219C>A	XP_006718621.1:p.Asp2073Glu
XM_006718559.2:c.6114C>A	XP_006718622.1:p.Asp2038Glu
XM_006718560.2:c.6111C>A	XP_006718623.1:p.Asp2037Glu
XM_006718561.2:c.6114C>A	XP_006718624.1:p.Asp2038Glu
XM_011545044.1:c.6228C>A	XP_011543346.1:p.Asp2076Glu
XM_011545045.1:c.6222C>A	XP_011543347.1:p.Asp2074Glu
XM_011545046.1:c.6195C>A	XP_011543348.1:p.Asp2065Glu
XM_011545047.1:c.6132C>A	XP_011543349.1:p.Asp2044Glu
XM_011545048.1:c.6003C>A	XP_011543350.1:p.Asp2001Glu
XM_011545049.1:c.5991C>A	XP_011543351.1:p.Asp1997Glu
XM_011545050.1:c.5964C>A	XP_011543352.1:p.Asp1988Glu
XM_011545051.1:c.6228C>A	XP_011543353.1:p.Asp2076Glu
XR_949938.1:n.6548C>A
XR_949941.1:n.6522C>A
XM_011545044.2:c.6228C>A	XP_011543346.1:p.Asp2076Glu
XM_011545046.2:c.6318C>A	XP_011543348.2:p.Asp2106Glu
XM_011545050.2:c.5964C>A	XP_011543352.1:p.Asp1988Glu
XM_017017778.1:c.6312C>A	XP_016873267.1:p.Asp2104Glu
XM_017017779.1:c.6309C>A	XP_016873268.1:p.Asp2103Glu
XM_017017780.1:c.6318C>A	XP_016873269.1:p.Asp2106Glu
XM_017017781.1:c.6222C>A	XP_016873270.1:p.Asp2074Glu
XM_017017782.1:c.6204C>A	XP_016873271.1:p.Asp2068Glu
XM_017017783.1:c.6201C>A	XP_016873272.1:p.Asp2067Glu
XM_017017784.1:c.6201C>A	XP_016873273.1:p.Asp2067Glu
XM_017017785.1:c.6081C>A	XP_016873274.1:p.Asp2027Glu
XM_017017786.1:c.6318C>A	XP_016873275.1:p.Asp2106Glu
XM_017017788.1:c.6204C>A	XP_016873277.1:p.Asp2068Glu
XR_001747885.1:n.6307C>A
XR_001747887.1:n.6293C>A
NM_000260.4:c.6228C>A MANE Select	NP_000251.3:p.Asp2076Glu
NM_001127180.2:c.6114C>A	NP_001120652.1:p.Asp2038Glu
NM_001369365.1:c.6081C>A	NP_001356294.1:p.Asp2027Glu