Canonical Allele Identifier: CA381936227

Gene: MYO7A

Linked Data

• dbSNP Id: rs371848786
• gnomAD v2: 11-76922353-C-G
• gnomAD v4: 11-77211308-C-G
• MyVariant Identifiers: chr11:g.76922353C>G (hg19) ; chr11:g.77211308C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211308C>G , CM000673.2:g.77211308C>G	GRCh38
NC_000011.9:g.76922353C>G , CM000673.1:g.76922353C>G	GRCh37
NC_000011.8:g.76600001C>G	NCBI36
NG_009086.1:g.88044C>G
NG_009086.2:g.88063C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6208C>G MANE Select	ENSP00000386331.3:p.Arg2070Gly
ENST00000670577.1:c.4009C>G
ENST00000409619.6:c.6061C>G	ENSP00000386635.2:p.Arg2021Gly
ENST00000409709.7:c.6208C>G	ENSP00000386331.3:p.Arg2070Gly
ENST00000458169.2:c.3634C>G	ENSP00000417017.2:p.Arg1212Gly
ENST00000458637.6:c.6094C>G	ENSP00000392185.2:p.Arg2032Gly
ENST00000481328.7:n.3744C>G
ENST00000526863.2:n.25+397C>G
ENST00000605744.1:n.1675C>G
NM_000260.3:c.6208C>G	NP_000251.3:p.Arg2070Gly
NM_001127180.1:c.6094C>G	NP_001120652.1:p.Arg2032Gly
XM_005274012.2:c.6091C>G	XP_005274069.1:p.Arg2031Gly
XM_006718558.2:c.6199C>G	XP_006718621.1:p.Arg2067Gly
XM_006718559.2:c.6094C>G	XP_006718622.1:p.Arg2032Gly
XM_006718560.2:c.6091C>G	XP_006718623.1:p.Arg2031Gly
XM_006718561.2:c.6094C>G	XP_006718624.1:p.Arg2032Gly
XM_011545044.1:c.6208C>G	XP_011543346.1:p.Arg2070Gly
XM_011545045.1:c.6202C>G	XP_011543347.1:p.Arg2068Gly
XM_011545046.1:c.6175C>G	XP_011543348.1:p.Arg2059Gly
XM_011545047.1:c.6112C>G	XP_011543349.1:p.Arg2038Gly
XM_011545048.1:c.5983C>G	XP_011543350.1:p.Arg1995Gly
XM_011545049.1:c.5971C>G	XP_011543351.1:p.Arg1991Gly
XM_011545050.1:c.5944C>G	XP_011543352.1:p.Arg1982Gly
XM_011545051.1:c.6208C>G	XP_011543353.1:p.Arg2070Gly
XR_949938.1:n.6528C>G
XR_949941.1:n.6502C>G
XM_011545044.2:c.6208C>G	XP_011543346.1:p.Arg2070Gly
XM_011545046.2:c.6298C>G	XP_011543348.2:p.Arg2100Gly
XM_011545050.2:c.5944C>G	XP_011543352.1:p.Arg1982Gly
XM_017017778.1:c.6292C>G	XP_016873267.1:p.Arg2098Gly
XM_017017779.1:c.6289C>G	XP_016873268.1:p.Arg2097Gly
XM_017017780.1:c.6298C>G	XP_016873269.1:p.Arg2100Gly
XM_017017781.1:c.6202C>G	XP_016873270.1:p.Arg2068Gly
XM_017017782.1:c.6184C>G	XP_016873271.1:p.Arg2062Gly
XM_017017783.1:c.6181C>G	XP_016873272.1:p.Arg2061Gly
XM_017017784.1:c.6181C>G	XP_016873273.1:p.Arg2061Gly
XM_017017785.1:c.6061C>G	XP_016873274.1:p.Arg2021Gly
XM_017017786.1:c.6298C>G	XP_016873275.1:p.Arg2100Gly
XM_017017788.1:c.6184C>G	XP_016873277.1:p.Arg2062Gly
XR_001747885.1:n.6287C>G
XR_001747887.1:n.6273C>G
NM_000260.4:c.6208C>G MANE Select	NP_000251.3:p.Arg2070Gly
NM_001127180.2:c.6094C>G	NP_001120652.1:p.Arg2032Gly
NM_001369365.1:c.6061C>G	NP_001356294.1:p.Arg2021Gly