Canonical Allele Identifier: CA475792036

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76922340C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211295C>G , CM000673.2:g.77211295C>G	GRCh38
NC_000011.9:g.76922340C>G , CM000673.1:g.76922340C>G	GRCh37
NC_000011.8:g.76599988C>G	NCBI36
NG_009086.1:g.88031C>G
NG_009086.2:g.88050C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6195C>G MANE Select	ENSP00000386331.3:p.Pro2065=
ENST00000670577.1:c.3996C>G
ENST00000409619.6:c.6048C>G	ENSP00000386635.2:p.Pro2016=
ENST00000409709.7:c.6195C>G	ENSP00000386331.3:p.Pro2065=
ENST00000458169.2:c.3621C>G	ENSP00000417017.2:p.Pro1207=
ENST00000458637.6:c.6081C>G	ENSP00000392185.2:p.Pro2027=
ENST00000481328.7:n.3731C>G
ENST00000526863.2:n.25+384C>G
ENST00000605744.1:n.1662C>G
NM_000260.3:c.6195C>G	NP_000251.3:p.Pro2065=
NM_001127180.1:c.6081C>G	NP_001120652.1:p.Pro2027=
XM_005274012.2:c.6078C>G	XP_005274069.1:p.Pro2026=
XM_006718558.2:c.6186C>G	XP_006718621.1:p.Pro2062=
XM_006718559.2:c.6081C>G	XP_006718622.1:p.Pro2027=
XM_006718560.2:c.6078C>G	XP_006718623.1:p.Pro2026=
XM_006718561.2:c.6081C>G	XP_006718624.1:p.Pro2027=
XM_011545044.1:c.6195C>G	XP_011543346.1:p.Pro2065=
XM_011545045.1:c.6189C>G	XP_011543347.1:p.Pro2063=
XM_011545046.1:c.6162C>G	XP_011543348.1:p.Pro2054=
XM_011545047.1:c.6099C>G	XP_011543349.1:p.Pro2033=
XM_011545048.1:c.5970C>G	XP_011543350.1:p.Pro1990=
XM_011545049.1:c.5958C>G	XP_011543351.1:p.Pro1986=
XM_011545050.1:c.5931C>G	XP_011543352.1:p.Pro1977=
XM_011545051.1:c.6195C>G	XP_011543353.1:p.Pro2065=
XR_949938.1:n.6515C>G
XR_949941.1:n.6489C>G
XM_011545044.2:c.6195C>G	XP_011543346.1:p.Pro2065=
XM_011545046.2:c.6285C>G	XP_011543348.2:p.Pro2095=
XM_011545050.2:c.5931C>G	XP_011543352.1:p.Pro1977=
XM_017017778.1:c.6279C>G	XP_016873267.1:p.Pro2093=
XM_017017779.1:c.6276C>G	XP_016873268.1:p.Pro2092=
XM_017017780.1:c.6285C>G	XP_016873269.1:p.Pro2095=
XM_017017781.1:c.6189C>G	XP_016873270.1:p.Pro2063=
XM_017017782.1:c.6171C>G	XP_016873271.1:p.Pro2057=
XM_017017783.1:c.6168C>G	XP_016873272.1:p.Pro2056=
XM_017017784.1:c.6168C>G	XP_016873273.1:p.Pro2056=
XM_017017785.1:c.6048C>G	XP_016873274.1:p.Pro2016=
XM_017017786.1:c.6285C>G	XP_016873275.1:p.Pro2095=
XM_017017788.1:c.6171C>G	XP_016873277.1:p.Pro2057=
XR_001747885.1:n.6274C>G
XR_001747886.1:n.6215C>G
XR_001747887.1:n.6260C>G
NM_000260.4:c.6195C>G MANE Select	NP_000251.3:p.Pro2065=
NM_001127180.2:c.6081C>G	NP_001120652.1:p.Pro2027=
NM_001369365.1:c.6048C>G	NP_001356294.1:p.Pro2016=