Canonical Allele Identifier: CA2792785922

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77157100_77157101insAGAT , CM000673.2:g.77157100_77157101insAGAT	GRCh38
NC_000011.9:g.76868146_76868147insAGAT , CM000673.1:g.76868146_76868147insAGAT	GRCh37
NC_000011.8:g.76545794_76545795insAGAT	NCBI36
NG_009086.1:g.33837_33838insAGAT
NG_009086.2:g.33855_33856insAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.735+96_735+97insAGAT MANE Select	ENSP00000386331.3:n.735+96_735+97insAGAT
ENST00000409619.6:c.702+96_702+97insAGAT	ENSP00000386635.2:n.702+96_702+97insAGAT
ENST00000409709.7:c.735+96_735+97insAGAT	ENSP00000386331.3:n.735+96_735+97insAGAT
ENST00000409893.5:c.735+96_735+97insAGAT	ENSP00000386689.1:n.735+96_735+97insAGAT
ENST00000458637.6:c.735+96_735+97insAGAT	ENSP00000392185.2:n.735+96_735+97insAGAT
ENST00000620575.4:c.735+96_735+97insAGAT	ENSP00000477640.1:n.735+96_735+97insAGAT
NM_000260.3:c.735+96_735+97insAGAT	NP_000251.3:n.735+96_735+97insAGAT
NM_001127179.2:c.735+96_735+97insAGAT	NP_001120651.2:n.735+96_735+97insAGAT
NM_001127180.1:c.735+96_735+97insAGAT	NP_001120652.1:n.735+96_735+97insAGAT
XM_005274012.2:c.735+96_735+97insAGAT	XP_005274069.1:n.735+96_735+97insAGAT
XM_006718558.2:c.735+96_735+97insAGAT	XP_006718621.1:n.735+96_735+97insAGAT
XM_006718559.2:c.735+96_735+97insAGAT	XP_006718622.1:n.735+96_735+97insAGAT
XM_006718560.2:c.735+96_735+97insAGAT	XP_006718623.1:n.735+96_735+97insAGAT
XM_006718561.2:c.735+96_735+97insAGAT	XP_006718624.1:n.735+96_735+97insAGAT
XM_011545044.1:c.735+96_735+97insAGAT	XP_011543346.1:n.735+96_735+97insAGAT
XM_011545045.1:c.735+96_735+97insAGAT	XP_011543347.1:n.735+96_735+97insAGAT
XM_011545046.1:c.702+96_702+97insAGAT	XP_011543348.1:n.702+96_702+97insAGAT
XM_011545047.1:c.735+96_735+97insAGAT	XP_011543349.1:n.735+96_735+97insAGAT
XM_011545048.1:c.735+96_735+97insAGAT	XP_011543350.1:n.735+96_735+97insAGAT
XM_011545049.1:c.735+96_735+97insAGAT	XP_011543351.1:n.735+96_735+97insAGAT
XM_011545050.1:c.477+96_477+97insAGAT	XP_011543352.1:n.477+96_477+97insAGAT
XM_011545051.1:c.735+96_735+97insAGAT	XP_011543353.1:n.735+96_735+97insAGAT
XM_011545052.1:c.735+96_735+97insAGAT	XP_011543354.1:n.735+96_735+97insAGAT
XR_949938.1:n.1055+96_1055+97insAGAT
XR_949941.1:n.1055+96_1055+97insAGAT
XR_949942.1:n.1057+96_1057+97insAGAT
XR_949943.1:n.1057+96_1057+97insAGAT
XM_011545044.2:c.735+96_735+97insAGAT	XP_011543346.1:n.735+96_735+97insAGAT
XM_011545046.2:c.825+96_825+97insAGAT	XP_011543348.2:n.825+96_825+97insAGAT
XM_011545050.2:c.477+96_477+97insAGAT	XP_011543352.1:n.477+96_477+97insAGAT
XM_017017778.1:c.825+96_825+97insAGAT	XP_016873267.1:n.825+96_825+97insAGAT
XM_017017779.1:c.825+96_825+97insAGAT	XP_016873268.1:n.825+96_825+97insAGAT
XM_017017780.1:c.825+96_825+97insAGAT	XP_016873269.1:n.825+96_825+97insAGAT
XM_017017781.1:c.825+96_825+97insAGAT	XP_016873270.1:n.825+96_825+97insAGAT
XM_017017782.1:c.825+96_825+97insAGAT	XP_016873271.1:n.825+96_825+97insAGAT
XM_017017783.1:c.825+96_825+97insAGAT	XP_016873272.1:n.825+96_825+97insAGAT
XM_017017784.1:c.825+96_825+97insAGAT	XP_016873273.1:n.825+96_825+97insAGAT
XM_017017785.1:c.825+96_825+97insAGAT	XP_016873274.1:n.825+96_825+97insAGAT
XM_017017786.1:c.825+96_825+97insAGAT	XP_016873275.1:n.825+96_825+97insAGAT
XM_017017787.1:c.825+96_825+97insAGAT	XP_016873276.1:n.825+96_825+97insAGAT
XM_017017788.1:c.825+96_825+97insAGAT	XP_016873277.1:n.825+96_825+97insAGAT
XR_001747885.1:n.840+96_840+97insAGAT
XR_001747886.1:n.840+96_840+97insAGAT
XR_001747887.1:n.840+96_840+97insAGAT
XR_001747888.1:n.840+96_840+97insAGAT
XR_001747889.1:n.840+96_840+97insAGAT
NM_000260.4:c.735+96_735+97insAGAT MANE Select	NP_000251.3:n.735+96_735+97insAGAT
NM_001127180.2:c.735+96_735+97insAGAT	NP_001120652.1:n.735+96_735+97insAGAT
NM_001369365.1:c.702+96_702+97insAGAT	NP_001356294.1:n.702+96_702+97insAGAT