Canonical Allele Identifier: CA2615262118

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77211052-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211054del , CM000673.2:g.77211054del	GRCh38
NC_000011.9:g.76922099del , CM000673.1:g.76922099del	GRCh37
NC_000011.8:g.76599747del	NCBI36
NG_009086.1:g.87790del
NG_009086.2:g.87809del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6052-98del MANE Select	ENSP00000386331.3:n.6052-98del
ENST00000670577.1:c.3853-98del
ENST00000409619.6:c.5905-98del	ENSP00000386635.2:n.5905-98del
ENST00000409709.7:c.6052-98del	ENSP00000386331.3:n.6052-98del
ENST00000458169.2:c.3478-98del	ENSP00000417017.2:n.3478-98del
ENST00000458637.6:c.5938-98del	ENSP00000392185.2:n.5938-98del
ENST00000481328.7:n.3588-98del
ENST00000526863.2:n.25+143del
ENST00000605744.1:n.1519-98del
NM_000260.3:c.6052-98del	NP_000251.3:n.6052-98del
NM_001127180.1:c.5938-98del	NP_001120652.1:n.5938-98del
XM_005274012.2:c.5935-98del	XP_005274069.1:n.5935-98del
XM_006718558.2:c.6043-98del	XP_006718621.1:n.6043-98del
XM_006718559.2:c.5938-98del	XP_006718622.1:n.5938-98del
XM_006718560.2:c.5935-98del	XP_006718623.1:n.5935-98del
XM_006718561.2:c.5938-98del	XP_006718624.1:n.5938-98del
XM_011545044.1:c.6052-98del	XP_011543346.1:n.6052-98del
XM_011545045.1:c.6046-98del	XP_011543347.1:n.6046-98del
XM_011545046.1:c.6019-98del	XP_011543348.1:n.6019-98del
XM_011545047.1:c.5956-98del	XP_011543349.1:n.5956-98del
XM_011545048.1:c.5827-98del	XP_011543350.1:n.5827-98del
XM_011545049.1:c.5815-98del	XP_011543351.1:n.5815-98del
XM_011545050.1:c.5788-98del	XP_011543352.1:n.5788-98del
XM_011545051.1:c.6052-98del	XP_011543353.1:n.6052-98del
XR_949938.1:n.6372-98del
XR_949941.1:n.6346-98del
XM_011545044.2:c.6052-98del	XP_011543346.1:n.6052-98del
XM_011545046.2:c.6142-98del	XP_011543348.2:n.6142-98del
XM_011545050.2:c.5788-98del	XP_011543352.1:n.5788-98del
XM_017017778.1:c.6136-98del	XP_016873267.1:n.6136-98del
XM_017017779.1:c.6133-98del	XP_016873268.1:n.6133-98del
XM_017017780.1:c.6142-98del	XP_016873269.1:n.6142-98del
XM_017017781.1:c.6046-98del	XP_016873270.1:n.6046-98del
XM_017017782.1:c.6028-98del	XP_016873271.1:n.6028-98del
XM_017017783.1:c.6025-98del	XP_016873272.1:n.6025-98del
XM_017017784.1:c.6025-98del	XP_016873273.1:n.6025-98del
XM_017017785.1:c.5905-98del	XP_016873274.1:n.5905-98del
XM_017017786.1:c.6142-98del	XP_016873275.1:n.6142-98del
XM_017017788.1:c.6028-98del	XP_016873277.1:n.6028-98del
XR_001747885.1:n.6131-98del
XR_001747886.1:n.6072-98del
XR_001747887.1:n.6117-98del
NM_000260.4:c.6052-98del MANE Select	NP_000251.3:n.6052-98del
NM_001127180.2:c.5938-98del	NP_001120652.1:n.5938-98del
NM_001369365.1:c.5905-98del	NP_001356294.1:n.5905-98del