Canonical Allele Identifier: CA475792070

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76922370T>C (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.6225T>C MANE Select	ENSP00000386331.3:p.Asp2075=
ENST00000670577.1:c.4026T>C
ENST00000409619.6:c.6078T>C	ENSP00000386635.2:p.Asp2026=
ENST00000409709.7:c.6225T>C	ENSP00000386331.3:p.Asp2075=
ENST00000458169.2:c.3651T>C	ENSP00000417017.2:p.Asp1217=
ENST00000458637.6:c.6111T>C	ENSP00000392185.2:p.Asp2037=
ENST00000481328.7:n.3761T>C
ENST00000526863.2:n.25+414T>C
ENST00000605744.1:n.1692T>C
NM_000260.3:c.6225T>C	NP_000251.3:p.Asp2075=
NM_001127180.1:c.6111T>C	NP_001120652.1:p.Asp2037=
XM_005274012.2:c.6108T>C	XP_005274069.1:p.Asp2036=
XM_006718558.2:c.6216T>C	XP_006718621.1:p.Asp2072=
XM_006718559.2:c.6111T>C	XP_006718622.1:p.Asp2037=
XM_006718560.2:c.6108T>C	XP_006718623.1:p.Asp2036=
XM_006718561.2:c.6111T>C	XP_006718624.1:p.Asp2037=
XM_011545044.1:c.6225T>C	XP_011543346.1:p.Asp2075=
XM_011545045.1:c.6219T>C	XP_011543347.1:p.Asp2073=
XM_011545046.1:c.6192T>C	XP_011543348.1:p.Asp2064=
XM_011545047.1:c.6129T>C	XP_011543349.1:p.Asp2043=
XM_011545048.1:c.6000T>C	XP_011543350.1:p.Asp2000=
XM_011545049.1:c.5988T>C	XP_011543351.1:p.Asp1996=
XM_011545050.1:c.5961T>C	XP_011543352.1:p.Asp1987=
XM_011545051.1:c.6225T>C	XP_011543353.1:p.Asp2075=
XR_949938.1:n.6545T>C
XR_949941.1:n.6519T>C
XM_011545044.2:c.6225T>C	XP_011543346.1:p.Asp2075=
XM_011545046.2:c.6315T>C	XP_011543348.2:p.Asp2105=
XM_011545050.2:c.5961T>C	XP_011543352.1:p.Asp1987=
XM_017017778.1:c.6309T>C	XP_016873267.1:p.Asp2103=
XM_017017779.1:c.6306T>C	XP_016873268.1:p.Asp2102=
XM_017017780.1:c.6315T>C	XP_016873269.1:p.Asp2105=
XM_017017781.1:c.6219T>C	XP_016873270.1:p.Asp2073=
XM_017017782.1:c.6201T>C	XP_016873271.1:p.Asp2067=
XM_017017783.1:c.6198T>C	XP_016873272.1:p.Asp2066=
XM_017017784.1:c.6198T>C	XP_016873273.1:p.Asp2066=
XM_017017785.1:c.6078T>C	XP_016873274.1:p.Asp2026=
XM_017017786.1:c.6315T>C	XP_016873275.1:p.Asp2105=
XM_017017788.1:c.6201T>C	XP_016873277.1:p.Asp2067=
XR_001747885.1:n.6304T>C
XR_001747887.1:n.6290T>C
NM_000260.4:c.6225T>C MANE Select	NP_000251.3:p.Asp2075=
NM_001127180.2:c.6111T>C	NP_001120652.1:p.Asp2037=
NM_001369365.1:c.6078T>C	NP_001356294.1:p.Asp2026=