Canonical Allele Identifier: CA475791716

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77208794-C-T
• MyVariant Identifiers: chr11:g.76919839C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77208794C>T , CM000673.2:g.77208794C>T	GRCh38
NC_000011.9:g.76919839C>T , CM000673.1:g.76919839C>T	GRCh37
NC_000011.8:g.76597487C>T	NCBI36
NG_009086.1:g.85530C>T
NG_009086.2:g.85549C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.6042C>T MANE Select	ENSP00000386331.3:p.His2014=
ENST00000670577.1:c.3843C>T
ENST00000409619.6:c.5895C>T	ENSP00000386635.2:p.His1965=
ENST00000409709.7:c.6042C>T	ENSP00000386331.3:p.His2014=
ENST00000458169.2:c.3468C>T	ENSP00000417017.2:p.His1156=
ENST00000458637.6:c.5928C>T	ENSP00000392185.2:p.His1976=
ENST00000481328.7:n.3578C>T
ENST00000605744.1:n.956C>T
NM_000260.3:c.6042C>T	NP_000251.3:p.His2014=
NM_001127180.1:c.5928C>T	NP_001120652.1:p.His1976=
XM_005274012.2:c.5925C>T	XP_005274069.1:p.His1975=
XM_006718558.2:c.6033C>T	XP_006718621.1:p.His2011=
XM_006718559.2:c.5928C>T	XP_006718622.1:p.His1976=
XM_006718560.2:c.5925C>T	XP_006718623.1:p.His1975=
XM_006718561.2:c.5928C>T	XP_006718624.1:p.His1976=
XM_011545044.1:c.6042C>T	XP_011543346.1:p.His2014=
XM_011545045.1:c.6036C>T	XP_011543347.1:p.His2012=
XM_011545046.1:c.6009C>T	XP_011543348.1:p.His2003=
XM_011545047.1:c.5946C>T	XP_011543349.1:p.His1982=
XM_011545048.1:c.5817C>T	XP_011543350.1:p.His1939=
XM_011545049.1:c.5805C>T	XP_011543351.1:p.His1935=
XM_011545050.1:c.5778C>T	XP_011543352.1:p.His1926=
XM_011545051.1:c.6042C>T	XP_011543353.1:p.His2014=
XR_949938.1:n.6362C>T
XR_949941.1:n.6336C>T
XM_011545044.2:c.6042C>T	XP_011543346.1:p.His2014=
XM_011545046.2:c.6132C>T	XP_011543348.2:p.His2044=
XM_011545050.2:c.5778C>T	XP_011543352.1:p.His1926=
XM_017017778.1:c.6126C>T	XP_016873267.1:p.His2042=
XM_017017779.1:c.6123C>T	XP_016873268.1:p.His2041=
XM_017017780.1:c.6132C>T	XP_016873269.1:p.His2044=
XM_017017781.1:c.6036C>T	XP_016873270.1:p.His2012=
XM_017017782.1:c.6018C>T	XP_016873271.1:p.His2006=
XM_017017783.1:c.6015C>T	XP_016873272.1:p.His2005=
XM_017017784.1:c.6015C>T	XP_016873273.1:p.His2005=
XM_017017785.1:c.5895C>T	XP_016873274.1:p.His1965=
XM_017017786.1:c.6132C>T	XP_016873275.1:p.His2044=
XM_017017788.1:c.6018C>T	XP_016873277.1:p.His2006=
XR_001747885.1:n.6121C>T
XR_001747886.1:n.6062C>T
XR_001747887.1:n.6107C>T
NM_000260.4:c.6042C>T MANE Select	NP_000251.3:p.His2014=
NM_001127180.2:c.5928C>T	NP_001120652.1:p.His1976=
NM_001369365.1:c.5895C>T	NP_001356294.1:p.His1965=