Canonical Allele Identifier: CA2835866075

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77189088del , CM000673.2:g.77189088del	GRCh38
NC_000011.9:g.76900133del , CM000673.1:g.76900133del	GRCh37
NC_000011.8:g.76577781del	NCBI36
NG_009086.1:g.65824del
NG_009086.2:g.65843del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.3504-256del MANE Select	ENSP00000386331.3:n.3504-256del
ENST00000670577.1:c.1345-256del
ENST00000409619.6:c.3471-256del	ENSP00000386635.2:n.3471-256del
ENST00000409709.7:c.3504-256del	ENSP00000386331.3:n.3504-256del
ENST00000458169.2:c.1047-256del	ENSP00000417017.2:n.1047-256del
ENST00000458637.6:c.3504-256del	ENSP00000392185.2:n.3504-256del
ENST00000467137.1:n.31-256del
ENST00000481328.7:n.1047-256del
NM_000260.3:c.3504-256del	NP_000251.3:n.3504-256del
NM_001127180.1:c.3504-256del	NP_001120652.1:n.3504-256del
XM_005274012.2:c.3504-256del	XP_005274069.1:n.3504-256del
XM_006718558.2:c.3504-256del	XP_006718621.1:n.3504-256del
XM_006718559.2:c.3504-256del	XP_006718622.1:n.3504-256del
XM_006718560.2:c.3504-256del	XP_006718623.1:n.3504-256del
XM_006718561.2:c.3504-256del	XP_006718624.1:n.3504-256del
XM_011545044.1:c.3504-256del	XP_011543346.1:n.3504-256del
XM_011545045.1:c.3504-256del	XP_011543347.1:n.3504-256del
XM_011545046.1:c.3471-256del	XP_011543348.1:n.3471-256del
XM_011545047.1:c.3414-256del	XP_011543349.1:n.3414-256del
XM_011545048.1:c.3285-256del	XP_011543350.1:n.3285-256del
XM_011545049.1:c.3273-256del	XP_011543351.1:n.3273-256del
XM_011545050.1:c.3246-256del	XP_011543352.1:n.3246-256del
XM_011545051.1:c.3504-256del	XP_011543353.1:n.3504-256del
XM_011545052.1:c.3504-256del	XP_011543354.1:n.3504-256del
XR_949938.1:n.3824-256del
XR_949941.1:n.3824-256del
XR_949942.1:n.3826-256del
XR_949943.1:n.3826-256del
XM_011545044.2:c.3504-256del	XP_011543346.1:n.3504-256del
XM_011545046.2:c.3594-256del	XP_011543348.2:n.3594-256del
XM_011545050.2:c.3246-256del	XP_011543352.1:n.3246-256del
XM_017017778.1:c.3594-256del	XP_016873267.1:n.3594-256del
XM_017017779.1:c.3594-256del	XP_016873268.1:n.3594-256del
XM_017017780.1:c.3594-256del	XP_016873269.1:n.3594-256del
XM_017017781.1:c.3504-256del	XP_016873270.1:n.3504-256del
XM_017017782.1:c.3594-256del	XP_016873271.1:n.3594-256del
XM_017017783.1:c.3594-256del	XP_016873272.1:n.3594-256del
XM_017017784.1:c.3594-256del	XP_016873273.1:n.3594-256del
XM_017017785.1:c.3363-256del	XP_016873274.1:n.3363-256del
XM_017017786.1:c.3594-256del	XP_016873275.1:n.3594-256del
XM_017017787.1:c.3594-256del	XP_016873276.1:n.3594-256del
XM_017017788.1:c.3594-256del	XP_016873277.1:n.3594-256del
XR_001747885.1:n.3609-256del
XR_001747886.1:n.3609-256del
XR_001747887.1:n.3609-256del
XR_001747888.1:n.3609-256del
XR_001747889.1:n.3609-256del
NM_000260.4:c.3504-256del MANE Select	NP_000251.3:n.3504-256del
NM_001127180.2:c.3504-256del	NP_001120652.1:n.3504-256del
NM_001369365.1:c.3471-256del	NP_001356294.1:n.3471-256del