Canonical Allele Identifier: CA381944184
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1402203
ClinVar RCV Id: RCV001925058
dbSNP Id: rs1373846137
MyVariant Identifiers: chr11:g.77182087C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77182087C>T , CM000673.2:g.77182087C>T GRCh38
NC_000011.8:g.76570781C>T NCBI36
NG_009086.1:g.58824C>T
NG_009086.2:g.58842C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.3041C>T MANE Select ENSP00000386331.3:p.Thr1014Met
ENST00000409893.6:c.1106C>T ENSP00000386689.2:p.Thr369Met
ENST00000670577.1:c.882C>T
ENST00000409619.6:c.3008C>T ENSP00000386635.2:p.Thr1003Met
ENST00000409709.7:c.3041C>T ENSP00000386331.3:p.Thr1014Met
ENST00000409893.5:c.3041C>T ENSP00000386689.1:p.Thr1014Met
ENST00000458169.2:c.584C>T ENSP00000417017.2:p.Thr195Met
ENST00000458637.6:c.3041C>T ENSP00000392185.2:p.Thr1014Met
ENST00000481328.7:n.584C>T
ENST00000620575.4:c.3041C>T ENSP00000477640.1:p.Thr1014Met
NM_000260.3:c.3041C>T NP_000251.3:p.Thr1014Met
NM_001127179.2:c.3041C>T NP_001120651.2:p.Thr1014Met
NM_001127180.1:c.3041C>T NP_001120652.1:p.Thr1014Met
XM_005274012.2:c.3041C>T XP_005274069.1:p.Thr1014Met
XM_006718558.2:c.3041C>T XP_006718621.1:p.Thr1014Met
XM_006718559.2:c.3041C>T XP_006718622.1:p.Thr1014Met
XM_006718560.2:c.3041C>T XP_006718623.1:p.Thr1014Met
XM_006718561.2:c.3041C>T XP_006718624.1:p.Thr1014Met
XM_011545044.1:c.3041C>T XP_011543346.1:p.Thr1014Met
XM_011545045.1:c.3041C>T XP_011543347.1:p.Thr1014Met
XM_011545046.1:c.3008C>T XP_011543348.1:p.Thr1003Met
XM_011545047.1:c.3041C>T XP_011543349.1:p.Thr1014Met
XM_011545048.1:c.2822C>T XP_011543350.1:p.Thr941Met
XM_011545049.1:c.2810C>T XP_011543351.1:p.Thr937Met
XM_011545050.1:c.2783C>T XP_011543352.1:p.Thr928Met
XM_011545051.1:c.3041C>T XP_011543353.1:p.Thr1014Met
XM_011545052.1:c.3041C>T XP_011543354.1:p.Thr1014Met
XR_949938.1:n.3361C>T
XR_949941.1:n.3361C>T
XR_949942.1:n.3363C>T
XR_949943.1:n.3363C>T
XM_011545044.2:c.3041C>T XP_011543346.1:p.Thr1014Met
XM_011545046.2:c.3131C>T XP_011543348.2:p.Thr1044Met
XM_011545050.2:c.2783C>T XP_011543352.1:p.Thr928Met
XM_017017778.1:c.3131C>T XP_016873267.1:p.Thr1044Met
XM_017017779.1:c.3131C>T XP_016873268.1:p.Thr1044Met
XM_017017780.1:c.3131C>T XP_016873269.1:p.Thr1044Met
XM_017017781.1:c.3131C>T XP_016873270.1:p.Thr1044Met
XM_017017782.1:c.3131C>T XP_016873271.1:p.Thr1044Met
XM_017017783.1:c.3131C>T XP_016873272.1:p.Thr1044Met
XM_017017784.1:c.3131C>T XP_016873273.1:p.Thr1044Met
XM_017017785.1:c.2900C>T XP_016873274.1:p.Thr967Met
XM_017017786.1:c.3131C>T XP_016873275.1:p.Thr1044Met
XM_017017787.1:c.3131C>T XP_016873276.1:p.Thr1044Met
XM_017017788.1:c.3131C>T XP_016873277.1:p.Thr1044Met
XR_001747885.1:n.3146C>T
XR_001747886.1:n.3146C>T
XR_001747887.1:n.3146C>T
XR_001747888.1:n.3146C>T
XR_001747889.1:n.3146C>T
NM_000260.4:c.3041C>T MANE Select NP_000251.3:p.Thr1014Met
NM_001127180.2:c.3041C>T NP_001120652.1:p.Thr1014Met
NM_001369365.1:c.3008C>T NP_001356294.1:p.Thr1003Met