Canonical Allele Identifier: CA381953890

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76918352A>C (hg19) ; chr11:g.77207307A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207307A>C , CM000673.2:g.77207307A>C	GRCh38
NC_000011.9:g.76918352A>C , CM000673.1:g.76918352A>C	GRCh37
NC_000011.8:g.76596000A>C	NCBI36
NG_009086.1:g.84043A>C
NG_009086.2:g.84062A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5761A>C MANE Select	ENSP00000386331.3:p.Ser1921Arg
ENST00000670577.1:c.3588A>C
ENST00000409619.6:c.5614A>C	ENSP00000386635.2:p.Ser1872Arg
ENST00000409709.7:c.5761A>C	ENSP00000386331.3:p.Ser1921Arg
ENST00000458169.2:c.3187A>C	ENSP00000417017.2:p.Ser1063Arg
ENST00000458637.6:c.5647A>C	ENSP00000392185.2:p.Ser1883Arg
ENST00000481328.7:n.3297A>C
ENST00000605744.1:n.675A>C
NM_000260.3:c.5761A>C	NP_000251.3:p.Ser1921Arg
NM_001127180.1:c.5647A>C	NP_001120652.1:p.Ser1883Arg
XM_005274012.2:c.5644A>C	XP_005274069.1:p.Ser1882Arg
XM_006718558.2:c.5752A>C	XP_006718621.1:p.Ser1918Arg
XM_006718559.2:c.5647A>C	XP_006718622.1:p.Ser1883Arg
XM_006718560.2:c.5644A>C	XP_006718623.1:p.Ser1882Arg
XM_006718561.2:c.5647A>C	XP_006718624.1:p.Ser1883Arg
XM_011545044.1:c.5761A>C	XP_011543346.1:p.Ser1921Arg
XM_011545045.1:c.5755A>C	XP_011543347.1:p.Ser1919Arg
XM_011545046.1:c.5728A>C	XP_011543348.1:p.Ser1910Arg
XM_011545047.1:c.5665A>C	XP_011543349.1:p.Ser1889Arg
XM_011545048.1:c.5536A>C	XP_011543350.1:p.Ser1846Arg
XM_011545049.1:c.5524A>C	XP_011543351.1:p.Ser1842Arg
XM_011545050.1:c.5497A>C	XP_011543352.1:p.Ser1833Arg
XM_011545051.1:c.5761A>C	XP_011543353.1:p.Ser1921Arg
XR_949938.1:n.6081A>C
XR_949941.1:n.6081A>C
XM_011545044.2:c.5761A>C	XP_011543346.1:p.Ser1921Arg
XM_011545046.2:c.5851A>C	XP_011543348.2:p.Ser1951Arg
XM_011545050.2:c.5497A>C	XP_011543352.1:p.Ser1833Arg
XM_017017778.1:c.5845A>C	XP_016873267.1:p.Ser1949Arg
XM_017017779.1:c.5842A>C	XP_016873268.1:p.Ser1948Arg
XM_017017780.1:c.5851A>C	XP_016873269.1:p.Ser1951Arg
XM_017017781.1:c.5755A>C	XP_016873270.1:p.Ser1919Arg
XM_017017782.1:c.5737A>C	XP_016873271.1:p.Ser1913Arg
XM_017017783.1:c.5734A>C	XP_016873272.1:p.Ser1912Arg
XM_017017784.1:c.5734A>C	XP_016873273.1:p.Ser1912Arg
XM_017017785.1:c.5614A>C	XP_016873274.1:p.Ser1872Arg
XM_017017786.1:c.5851A>C	XP_016873275.1:p.Ser1951Arg
XM_017017788.1:c.5737A>C	XP_016873277.1:p.Ser1913Arg
XR_001747885.1:n.5866A>C
XR_001747886.1:n.5781A>C
XR_001747887.1:n.5852A>C
NM_000260.4:c.5761A>C MANE Select	NP_000251.3:p.Ser1921Arg
NM_001127180.2:c.5647A>C	NP_001120652.1:p.Ser1883Arg
NM_001369365.1:c.5614A>C	NP_001356294.1:p.Ser1872Arg