Canonical Allele Identifier: CA224825214

Gene: MYO7A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77208460_77208462del , CM000673.2:g.77208460_77208462del	GRCh38
NC_000011.9:g.76919505_76919507del , CM000673.1:g.76919505_76919507del	GRCh37
NC_000011.8:g.76597153_76597155del	NCBI36
NG_009086.1:g.85196_85198del
NG_009086.2:g.85215_85217del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5887_5889del MANE Select	ENSP00000386331.3:p.Phe1963del
ENST00000670577.1:c.3714_3716del
ENST00000409619.6:c.5740_5742del	ENSP00000386635.2:p.Phe1914del
ENST00000409709.7:c.5887_5889del	ENSP00000386331.3:p.Phe1963del
ENST00000458169.2:c.3313_3315del	ENSP00000417017.2:p.Phe1105del
ENST00000458637.6:c.5773_5775del	ENSP00000392185.2:p.Phe1925del
ENST00000481328.7:n.3423_3425del
ENST00000605744.1:n.801_803del
NM_000260.3:c.5887_5889del	NP_000251.3:p.Phe1963del
NM_001127180.1:c.5773_5775del	NP_001120652.1:p.Phe1925del
XM_005274012.2:c.5770_5772del	XP_005274069.1:p.Phe1924del
XM_006718558.2:c.5878_5880del	XP_006718621.1:p.Phe1960del
XM_006718559.2:c.5773_5775del	XP_006718622.1:p.Phe1925del
XM_006718560.2:c.5770_5772del	XP_006718623.1:p.Phe1924del
XM_006718561.2:c.5773_5775del	XP_006718624.1:p.Phe1925del
XM_011545044.1:c.5887_5889del	XP_011543346.1:p.Phe1963del
XM_011545045.1:c.5881_5883del	XP_011543347.1:p.Phe1961del
XM_011545046.1:c.5854_5856del	XP_011543348.1:p.Phe1952del
XM_011545047.1:c.5791_5793del	XP_011543349.1:p.Phe1931del
XM_011545048.1:c.5662_5664del	XP_011543350.1:p.Phe1888del
XM_011545049.1:c.5650_5652del	XP_011543351.1:p.Phe1884del
XM_011545050.1:c.5623_5625del	XP_011543352.1:p.Phe1875del
XM_011545051.1:c.5887_5889del	XP_011543353.1:p.Phe1963del
XR_949938.1:n.6207_6209del
XR_949941.1:n.6207_6209del
XM_011545044.2:c.5887_5889del	XP_011543346.1:p.Phe1963del
XM_011545046.2:c.5977_5979del	XP_011543348.2:p.Phe1993del
XM_011545050.2:c.5623_5625del	XP_011543352.1:p.Phe1875del
XM_017017778.1:c.5971_5973del	XP_016873267.1:p.Phe1991del
XM_017017779.1:c.5968_5970del	XP_016873268.1:p.Phe1990del
XM_017017780.1:c.5977_5979del	XP_016873269.1:p.Phe1993del
XM_017017781.1:c.5881_5883del	XP_016873270.1:p.Phe1961del
XM_017017782.1:c.5863_5865del	XP_016873271.1:p.Phe1955del
XM_017017783.1:c.5860_5862del	XP_016873272.1:p.Phe1954del
XM_017017784.1:c.5860_5862del	XP_016873273.1:p.Phe1954del
XM_017017785.1:c.5740_5742del	XP_016873274.1:p.Phe1914del
XM_017017786.1:c.5977_5979del	XP_016873275.1:p.Phe1993del
XM_017017788.1:c.5863_5865del	XP_016873277.1:p.Phe1955del
XR_001747885.1:n.5992_5994del
XR_001747886.1:n.5907_5909del
XR_001747887.1:n.5978_5980del
NM_000260.4:c.5887_5889del MANE Select	NP_000251.3:p.Phe1963del
NM_001127180.2:c.5773_5775del	NP_001120652.1:p.Phe1925del
NM_001369365.1:c.5740_5742del	NP_001356294.1:p.Phe1914del