Canonical Allele Identifier: CA381935533

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77211173-G-A
• MyVariant Identifiers: chr11:g.76922218G>A (hg19) ; chr11:g.77211173G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211173G>A , CM000673.2:g.77211173G>A	GRCh38
NC_000011.9:g.76922218G>A , CM000673.1:g.76922218G>A	GRCh37
NC_000011.8:g.76599866G>A	NCBI36
NG_009086.1:g.87909G>A
NG_009086.2:g.87928G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6073G>A MANE Select	ENSP00000386331.3:p.Gly2025Ser
ENST00000670577.1:c.3874G>A
ENST00000409619.6:c.5926G>A	ENSP00000386635.2:p.Gly1976Ser
ENST00000409709.7:c.6073G>A	ENSP00000386331.3:p.Gly2025Ser
ENST00000458169.2:c.3499G>A	ENSP00000417017.2:p.Gly1167Ser
ENST00000458637.6:c.5959G>A	ENSP00000392185.2:p.Gly1987Ser
ENST00000481328.7:n.3609G>A
ENST00000526863.2:n.25+262G>A
ENST00000605744.1:n.1540G>A
NM_000260.3:c.6073G>A	NP_000251.3:p.Gly2025Ser
NM_001127180.1:c.5959G>A	NP_001120652.1:p.Gly1987Ser
XM_005274012.2:c.5956G>A	XP_005274069.1:p.Gly1986Ser
XM_006718558.2:c.6064G>A	XP_006718621.1:p.Gly2022Ser
XM_006718559.2:c.5959G>A	XP_006718622.1:p.Gly1987Ser
XM_006718560.2:c.5956G>A	XP_006718623.1:p.Gly1986Ser
XM_006718561.2:c.5959G>A	XP_006718624.1:p.Gly1987Ser
XM_011545044.1:c.6073G>A	XP_011543346.1:p.Gly2025Ser
XM_011545045.1:c.6067G>A	XP_011543347.1:p.Gly2023Ser
XM_011545046.1:c.6040G>A	XP_011543348.1:p.Gly2014Ser
XM_011545047.1:c.5977G>A	XP_011543349.1:p.Gly1993Ser
XM_011545048.1:c.5848G>A	XP_011543350.1:p.Gly1950Ser
XM_011545049.1:c.5836G>A	XP_011543351.1:p.Gly1946Ser
XM_011545050.1:c.5809G>A	XP_011543352.1:p.Gly1937Ser
XM_011545051.1:c.6073G>A	XP_011543353.1:p.Gly2025Ser
XR_949938.1:n.6393G>A
XR_949941.1:n.6367G>A
XM_011545044.2:c.6073G>A	XP_011543346.1:p.Gly2025Ser
XM_011545046.2:c.6163G>A	XP_011543348.2:p.Gly2055Ser
XM_011545050.2:c.5809G>A	XP_011543352.1:p.Gly1937Ser
XM_017017778.1:c.6157G>A	XP_016873267.1:p.Gly2053Ser
XM_017017779.1:c.6154G>A	XP_016873268.1:p.Gly2052Ser
XM_017017780.1:c.6163G>A	XP_016873269.1:p.Gly2055Ser
XM_017017781.1:c.6067G>A	XP_016873270.1:p.Gly2023Ser
XM_017017782.1:c.6049G>A	XP_016873271.1:p.Gly2017Ser
XM_017017783.1:c.6046G>A	XP_016873272.1:p.Gly2016Ser
XM_017017784.1:c.6046G>A	XP_016873273.1:p.Gly2016Ser
XM_017017785.1:c.5926G>A	XP_016873274.1:p.Gly1976Ser
XM_017017786.1:c.6163G>A	XP_016873275.1:p.Gly2055Ser
XM_017017788.1:c.6049G>A	XP_016873277.1:p.Gly2017Ser
XR_001747885.1:n.6152G>A
XR_001747886.1:n.6093G>A
XR_001747887.1:n.6138G>A
NM_000260.4:c.6073G>A MANE Select	NP_000251.3:p.Gly2025Ser
NM_001127180.2:c.5959G>A	NP_001120652.1:p.Gly1987Ser
NM_001369365.1:c.5926G>A	NP_001356294.1:p.Gly1976Ser