Canonical Allele Identifier: CA2792788279

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77210982_77211121del , CM000673.2:g.77210982_77211121del	GRCh38
NC_000011.9:g.76922027_76922166del , CM000673.1:g.76922027_76922166del	GRCh37
NC_000011.8:g.76599675_76599814del	NCBI36
NG_009086.1:g.87718_87857del
NG_009086.2:g.87737_87876del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6052-170_6052-31del MANE Select	ENSP00000386331.3:n.6052-170_6052-31del
ENST00000670577.1:c.3853-170_3853-31del
ENST00000409619.6:c.5905-170_5905-31del	ENSP00000386635.2:n.5905-170_5905-31del
ENST00000409709.7:c.6052-170_6052-31del	ENSP00000386331.3:n.6052-170_6052-31del
ENST00000458169.2:c.3478-170_3478-31del	ENSP00000417017.2:n.3478-170_3478-31del
ENST00000458637.6:c.5938-170_5938-31del	ENSP00000392185.2:n.5938-170_5938-31del
ENST00000481328.7:n.3588-170_3588-31del
ENST00000526863.2:n.25+71_25+210del
ENST00000605744.1:n.1519-170_1519-31del
NM_000260.3:c.6052-170_6052-31del	NP_000251.3:n.6052-170_6052-31del
NM_001127180.1:c.5938-170_5938-31del	NP_001120652.1:n.5938-170_5938-31del
XM_005274012.2:c.5935-170_5935-31del	XP_005274069.1:n.5935-170_5935-31del
XM_006718558.2:c.6043-170_6043-31del	XP_006718621.1:n.6043-170_6043-31del
XM_006718559.2:c.5938-170_5938-31del	XP_006718622.1:n.5938-170_5938-31del
XM_006718560.2:c.5935-170_5935-31del	XP_006718623.1:n.5935-170_5935-31del
XM_006718561.2:c.5938-170_5938-31del	XP_006718624.1:n.5938-170_5938-31del
XM_011545044.1:c.6052-170_6052-31del	XP_011543346.1:n.6052-170_6052-31del
XM_011545045.1:c.6046-170_6046-31del	XP_011543347.1:n.6046-170_6046-31del
XM_011545046.1:c.6019-170_6019-31del	XP_011543348.1:n.6019-170_6019-31del
XM_011545047.1:c.5956-170_5956-31del	XP_011543349.1:n.5956-170_5956-31del
XM_011545048.1:c.5827-170_5827-31del	XP_011543350.1:n.5827-170_5827-31del
XM_011545049.1:c.5815-170_5815-31del	XP_011543351.1:n.5815-170_5815-31del
XM_011545050.1:c.5788-170_5788-31del	XP_011543352.1:n.5788-170_5788-31del
XM_011545051.1:c.6052-170_6052-31del	XP_011543353.1:n.6052-170_6052-31del
XR_949938.1:n.6372-170_6372-31del
XR_949941.1:n.6346-170_6346-31del
XM_011545044.2:c.6052-170_6052-31del	XP_011543346.1:n.6052-170_6052-31del
XM_011545046.2:c.6142-170_6142-31del	XP_011543348.2:n.6142-170_6142-31del
XM_011545050.2:c.5788-170_5788-31del	XP_011543352.1:n.5788-170_5788-31del
XM_017017778.1:c.6136-170_6136-31del	XP_016873267.1:n.6136-170_6136-31del
XM_017017779.1:c.6133-170_6133-31del	XP_016873268.1:n.6133-170_6133-31del
XM_017017780.1:c.6142-170_6142-31del	XP_016873269.1:n.6142-170_6142-31del
XM_017017781.1:c.6046-170_6046-31del	XP_016873270.1:n.6046-170_6046-31del
XM_017017782.1:c.6028-170_6028-31del	XP_016873271.1:n.6028-170_6028-31del
XM_017017783.1:c.6025-170_6025-31del	XP_016873272.1:n.6025-170_6025-31del
XM_017017784.1:c.6025-170_6025-31del	XP_016873273.1:n.6025-170_6025-31del
XM_017017785.1:c.5905-170_5905-31del	XP_016873274.1:n.5905-170_5905-31del
XM_017017786.1:c.6142-170_6142-31del	XP_016873275.1:n.6142-170_6142-31del
XM_017017788.1:c.6028-170_6028-31del	XP_016873277.1:n.6028-170_6028-31del
XR_001747885.1:n.6131-170_6131-31del
XR_001747886.1:n.6072-170_6072-31del
XR_001747887.1:n.6117-170_6117-31del
NM_000260.4:c.6052-170_6052-31del MANE Select	NP_000251.3:n.6052-170_6052-31del
NM_001127180.2:c.5938-170_5938-31del	NP_001120652.1:n.5938-170_5938-31del
NM_001369365.1:c.5905-170_5905-31del	NP_001356294.1:n.5905-170_5905-31del