Canonical Allele Identifier: CA381953905

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76918355A>T (hg19) ; chr11:g.77207310A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207310A>T , CM000673.2:g.77207310A>T	GRCh38
NC_000011.9:g.76918355A>T , CM000673.1:g.76918355A>T	GRCh37
NC_000011.8:g.76596003A>T	NCBI36
NG_009086.1:g.84046A>T
NG_009086.2:g.84065A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5764A>T MANE Select	ENSP00000386331.3:p.Thr1922Ser
ENST00000670577.1:c.3591A>T
ENST00000409619.6:c.5617A>T	ENSP00000386635.2:p.Thr1873Ser
ENST00000409709.7:c.5764A>T	ENSP00000386331.3:p.Thr1922Ser
ENST00000458169.2:c.3190A>T	ENSP00000417017.2:p.Thr1064Ser
ENST00000458637.6:c.5650A>T	ENSP00000392185.2:p.Thr1884Ser
ENST00000481328.7:n.3300A>T
ENST00000605744.1:n.678A>T
NM_000260.3:c.5764A>T	NP_000251.3:p.Thr1922Ser
NM_001127180.1:c.5650A>T	NP_001120652.1:p.Thr1884Ser
XM_005274012.2:c.5647A>T	XP_005274069.1:p.Thr1883Ser
XM_006718558.2:c.5755A>T	XP_006718621.1:p.Thr1919Ser
XM_006718559.2:c.5650A>T	XP_006718622.1:p.Thr1884Ser
XM_006718560.2:c.5647A>T	XP_006718623.1:p.Thr1883Ser
XM_006718561.2:c.5650A>T	XP_006718624.1:p.Thr1884Ser
XM_011545044.1:c.5764A>T	XP_011543346.1:p.Thr1922Ser
XM_011545045.1:c.5758A>T	XP_011543347.1:p.Thr1920Ser
XM_011545046.1:c.5731A>T	XP_011543348.1:p.Thr1911Ser
XM_011545047.1:c.5668A>T	XP_011543349.1:p.Thr1890Ser
XM_011545048.1:c.5539A>T	XP_011543350.1:p.Thr1847Ser
XM_011545049.1:c.5527A>T	XP_011543351.1:p.Thr1843Ser
XM_011545050.1:c.5500A>T	XP_011543352.1:p.Thr1834Ser
XM_011545051.1:c.5764A>T	XP_011543353.1:p.Thr1922Ser
XR_949938.1:n.6084A>T
XR_949941.1:n.6084A>T
XM_011545044.2:c.5764A>T	XP_011543346.1:p.Thr1922Ser
XM_011545046.2:c.5854A>T	XP_011543348.2:p.Thr1952Ser
XM_011545050.2:c.5500A>T	XP_011543352.1:p.Thr1834Ser
XM_017017778.1:c.5848A>T	XP_016873267.1:p.Thr1950Ser
XM_017017779.1:c.5845A>T	XP_016873268.1:p.Thr1949Ser
XM_017017780.1:c.5854A>T	XP_016873269.1:p.Thr1952Ser
XM_017017781.1:c.5758A>T	XP_016873270.1:p.Thr1920Ser
XM_017017782.1:c.5740A>T	XP_016873271.1:p.Thr1914Ser
XM_017017783.1:c.5737A>T	XP_016873272.1:p.Thr1913Ser
XM_017017784.1:c.5737A>T	XP_016873273.1:p.Thr1913Ser
XM_017017785.1:c.5617A>T	XP_016873274.1:p.Thr1873Ser
XM_017017786.1:c.5854A>T	XP_016873275.1:p.Thr1952Ser
XM_017017788.1:c.5740A>T	XP_016873277.1:p.Thr1914Ser
XR_001747885.1:n.5869A>T
XR_001747886.1:n.5784A>T
XR_001747887.1:n.5855A>T
NM_000260.4:c.5764A>T MANE Select	NP_000251.3:p.Thr1922Ser
NM_001127180.2:c.5650A>T	NP_001120652.1:p.Thr1884Ser
NM_001369365.1:c.5617A>T	NP_001356294.1:p.Thr1873Ser