Canonical Allele Identifier: CA381936308

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76922370T>G (hg19) ; chr11:g.77211325T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211325T>G , CM000673.2:g.77211325T>G	GRCh38
NC_000011.9:g.76922370T>G , CM000673.1:g.76922370T>G	GRCh37
NC_000011.8:g.76600018T>G	NCBI36
NG_009086.1:g.88061T>G
NG_009086.2:g.88080T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6225T>G MANE Select	ENSP00000386331.3:p.Asp2075Glu
ENST00000670577.1:c.4026T>G
ENST00000409619.6:c.6078T>G	ENSP00000386635.2:p.Asp2026Glu
ENST00000409709.7:c.6225T>G	ENSP00000386331.3:p.Asp2075Glu
ENST00000458169.2:c.3651T>G	ENSP00000417017.2:p.Asp1217Glu
ENST00000458637.6:c.6111T>G	ENSP00000392185.2:p.Asp2037Glu
ENST00000481328.7:n.3761T>G
ENST00000526863.2:n.25+414T>G
ENST00000605744.1:n.1692T>G
NM_000260.3:c.6225T>G	NP_000251.3:p.Asp2075Glu
NM_001127180.1:c.6111T>G	NP_001120652.1:p.Asp2037Glu
XM_005274012.2:c.6108T>G	XP_005274069.1:p.Asp2036Glu
XM_006718558.2:c.6216T>G	XP_006718621.1:p.Asp2072Glu
XM_006718559.2:c.6111T>G	XP_006718622.1:p.Asp2037Glu
XM_006718560.2:c.6108T>G	XP_006718623.1:p.Asp2036Glu
XM_006718561.2:c.6111T>G	XP_006718624.1:p.Asp2037Glu
XM_011545044.1:c.6225T>G	XP_011543346.1:p.Asp2075Glu
XM_011545045.1:c.6219T>G	XP_011543347.1:p.Asp2073Glu
XM_011545046.1:c.6192T>G	XP_011543348.1:p.Asp2064Glu
XM_011545047.1:c.6129T>G	XP_011543349.1:p.Asp2043Glu
XM_011545048.1:c.6000T>G	XP_011543350.1:p.Asp2000Glu
XM_011545049.1:c.5988T>G	XP_011543351.1:p.Asp1996Glu
XM_011545050.1:c.5961T>G	XP_011543352.1:p.Asp1987Glu
XM_011545051.1:c.6225T>G	XP_011543353.1:p.Asp2075Glu
XR_949938.1:n.6545T>G
XR_949941.1:n.6519T>G
XM_011545044.2:c.6225T>G	XP_011543346.1:p.Asp2075Glu
XM_011545046.2:c.6315T>G	XP_011543348.2:p.Asp2105Glu
XM_011545050.2:c.5961T>G	XP_011543352.1:p.Asp1987Glu
XM_017017778.1:c.6309T>G	XP_016873267.1:p.Asp2103Glu
XM_017017779.1:c.6306T>G	XP_016873268.1:p.Asp2102Glu
XM_017017780.1:c.6315T>G	XP_016873269.1:p.Asp2105Glu
XM_017017781.1:c.6219T>G	XP_016873270.1:p.Asp2073Glu
XM_017017782.1:c.6201T>G	XP_016873271.1:p.Asp2067Glu
XM_017017783.1:c.6198T>G	XP_016873272.1:p.Asp2066Glu
XM_017017784.1:c.6198T>G	XP_016873273.1:p.Asp2066Glu
XM_017017785.1:c.6078T>G	XP_016873274.1:p.Asp2026Glu
XM_017017786.1:c.6315T>G	XP_016873275.1:p.Asp2105Glu
XM_017017788.1:c.6201T>G	XP_016873277.1:p.Asp2067Glu
XR_001747885.1:n.6304T>G
XR_001747887.1:n.6290T>G
NM_000260.4:c.6225T>G MANE Select	NP_000251.3:p.Asp2075Glu
NM_001127180.2:c.6111T>G	NP_001120652.1:p.Asp2037Glu
NM_001369365.1:c.6078T>G	NP_001356294.1:p.Asp2026Glu