Canonical Allele Identifier: CA381931332

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76867023T>G (hg19) ; chr11:g.77155977T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77155977T>G , CM000673.2:g.77155977T>G	GRCh38
NC_000011.9:g.76867023T>G , CM000673.1:g.76867023T>G	GRCh37
NC_000011.8:g.76544671T>G	NCBI36
NG_009086.1:g.32714T>G
NG_009086.2:g.32732T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.356T>G MANE Select	ENSP00000386331.3:p.Ile119Ser
ENST00000409619.6:c.323T>G	ENSP00000386635.2:p.Ile108Ser
ENST00000409709.7:c.356T>G	ENSP00000386331.3:p.Ile119Ser
ENST00000409893.5:c.356T>G	ENSP00000386689.1:p.Ile119Ser
ENST00000458637.6:c.356T>G	ENSP00000392185.2:p.Ile119Ser
ENST00000620575.4:c.356T>G	ENSP00000477640.1:p.Ile119Ser
NM_000260.3:c.356T>G	NP_000251.3:p.Ile119Ser
NM_001127179.2:c.356T>G	NP_001120651.2:p.Ile119Ser
NM_001127180.1:c.356T>G	NP_001120652.1:p.Ile119Ser
XM_005274012.2:c.356T>G	XP_005274069.1:p.Ile119Ser
XM_006718558.2:c.356T>G	XP_006718621.1:p.Ile119Ser
XM_006718559.2:c.356T>G	XP_006718622.1:p.Ile119Ser
XM_006718560.2:c.356T>G	XP_006718623.1:p.Ile119Ser
XM_006718561.2:c.356T>G	XP_006718624.1:p.Ile119Ser
XM_011545044.1:c.356T>G	XP_011543346.1:p.Ile119Ser
XM_011545045.1:c.356T>G	XP_011543347.1:p.Ile119Ser
XM_011545046.1:c.323T>G	XP_011543348.1:p.Ile108Ser
XM_011545047.1:c.356T>G	XP_011543349.1:p.Ile119Ser
XM_011545048.1:c.356T>G	XP_011543350.1:p.Ile119Ser
XM_011545049.1:c.356T>G	XP_011543351.1:p.Ile119Ser
XM_011545050.1:c.98T>G	XP_011543352.1:p.Ile33Ser
XM_011545051.1:c.356T>G	XP_011543353.1:p.Ile119Ser
XM_011545052.1:c.356T>G	XP_011543354.1:p.Ile119Ser
XR_949938.1:n.676T>G
XR_949941.1:n.676T>G
XR_949942.1:n.678T>G
XR_949943.1:n.678T>G
XM_011545044.2:c.356T>G	XP_011543346.1:p.Ile119Ser
XM_011545046.2:c.446T>G	XP_011543348.2:p.Ile149Ser
XM_011545050.2:c.98T>G	XP_011543352.1:p.Ile33Ser
XM_017017778.1:c.446T>G	XP_016873267.1:p.Ile149Ser
XM_017017779.1:c.446T>G	XP_016873268.1:p.Ile149Ser
XM_017017780.1:c.446T>G	XP_016873269.1:p.Ile149Ser
XM_017017781.1:c.446T>G	XP_016873270.1:p.Ile149Ser
XM_017017782.1:c.446T>G	XP_016873271.1:p.Ile149Ser
XM_017017783.1:c.446T>G	XP_016873272.1:p.Ile149Ser
XM_017017784.1:c.446T>G	XP_016873273.1:p.Ile149Ser
XM_017017785.1:c.446T>G	XP_016873274.1:p.Ile149Ser
XM_017017786.1:c.446T>G	XP_016873275.1:p.Ile149Ser
XM_017017787.1:c.446T>G	XP_016873276.1:p.Ile149Ser
XM_017017788.1:c.446T>G	XP_016873277.1:p.Ile149Ser
XR_001747885.1:n.461T>G
XR_001747886.1:n.461T>G
XR_001747887.1:n.461T>G
XR_001747888.1:n.461T>G
XR_001747889.1:n.461T>G
NM_000260.4:c.356T>G MANE Select	NP_000251.3:p.Ile119Ser
NM_001127180.2:c.356T>G	NP_001120652.1:p.Ile119Ser
NM_001369365.1:c.323T>G	NP_001356294.1:p.Ile108Ser