Canonical Allele Identifier: CA381954152

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76918443A>G (hg19) ; chr11:g.77207398A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207398A>G , CM000673.2:g.77207398A>G	GRCh38
NC_000011.9:g.76918443A>G , CM000673.1:g.76918443A>G	GRCh37
NC_000011.8:g.76596091A>G	NCBI36
NG_009086.1:g.84134A>G
NG_009086.2:g.84153A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5852A>G MANE Select	ENSP00000386331.3:p.Asp1951Gly
ENST00000670577.1:c.3679A>G
ENST00000409619.6:c.5705A>G	ENSP00000386635.2:p.Asp1902Gly
ENST00000409709.7:c.5852A>G	ENSP00000386331.3:p.Asp1951Gly
ENST00000458169.2:c.3278A>G	ENSP00000417017.2:p.Asp1093Gly
ENST00000458637.6:c.5738A>G	ENSP00000392185.2:p.Asp1913Gly
ENST00000481328.7:n.3388A>G
ENST00000605744.1:n.766A>G
NM_000260.3:c.5852A>G	NP_000251.3:p.Asp1951Gly
NM_001127180.1:c.5738A>G	NP_001120652.1:p.Asp1913Gly
XM_005274012.2:c.5735A>G	XP_005274069.1:p.Asp1912Gly
XM_006718558.2:c.5843A>G	XP_006718621.1:p.Asp1948Gly
XM_006718559.2:c.5738A>G	XP_006718622.1:p.Asp1913Gly
XM_006718560.2:c.5735A>G	XP_006718623.1:p.Asp1912Gly
XM_006718561.2:c.5738A>G	XP_006718624.1:p.Asp1913Gly
XM_011545044.1:c.5852A>G	XP_011543346.1:p.Asp1951Gly
XM_011545045.1:c.5846A>G	XP_011543347.1:p.Asp1949Gly
XM_011545046.1:c.5819A>G	XP_011543348.1:p.Asp1940Gly
XM_011545047.1:c.5756A>G	XP_011543349.1:p.Asp1919Gly
XM_011545048.1:c.5627A>G	XP_011543350.1:p.Asp1876Gly
XM_011545049.1:c.5615A>G	XP_011543351.1:p.Asp1872Gly
XM_011545050.1:c.5588A>G	XP_011543352.1:p.Asp1863Gly
XM_011545051.1:c.5852A>G	XP_011543353.1:p.Asp1951Gly
XR_949938.1:n.6172A>G
XR_949941.1:n.6172A>G
XM_011545044.2:c.5852A>G	XP_011543346.1:p.Asp1951Gly
XM_011545046.2:c.5942A>G	XP_011543348.2:p.Asp1981Gly
XM_011545050.2:c.5588A>G	XP_011543352.1:p.Asp1863Gly
XM_017017778.1:c.5936A>G	XP_016873267.1:p.Asp1979Gly
XM_017017779.1:c.5933A>G	XP_016873268.1:p.Asp1978Gly
XM_017017780.1:c.5942A>G	XP_016873269.1:p.Asp1981Gly
XM_017017781.1:c.5846A>G	XP_016873270.1:p.Asp1949Gly
XM_017017782.1:c.5828A>G	XP_016873271.1:p.Asp1943Gly
XM_017017783.1:c.5825A>G	XP_016873272.1:p.Asp1942Gly
XM_017017784.1:c.5825A>G	XP_016873273.1:p.Asp1942Gly
XM_017017785.1:c.5705A>G	XP_016873274.1:p.Asp1902Gly
XM_017017786.1:c.5942A>G	XP_016873275.1:p.Asp1981Gly
XM_017017788.1:c.5828A>G	XP_016873277.1:p.Asp1943Gly
XR_001747885.1:n.5957A>G
XR_001747886.1:n.5872A>G
XR_001747887.1:n.5943A>G
NM_000260.4:c.5852A>G MANE Select	NP_000251.3:p.Asp1951Gly
NM_001127180.2:c.5738A>G	NP_001120652.1:p.Asp1913Gly
NM_001369365.1:c.5705A>G	NP_001356294.1:p.Asp1902Gly