Canonical Allele Identifier: CA1984127916

Gene: MYO7A

Linked Data

• dbSNP Id: rs1957524733
• gnomAD v4: 11-77207440-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207440G>T , CM000673.2:g.77207440G>T	GRCh38
NC_000011.9:g.76918485G>T , CM000673.1:g.76918485G>T	GRCh37
NC_000011.8:g.76596133G>T	NCBI36
NG_009086.1:g.84176G>T
NG_009086.2:g.84195G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5856+38G>T MANE Select	ENSP00000386331.3:n.5856+38G>T
ENST00000670577.1:c.3683+38G>T
ENST00000409619.6:c.5709+38G>T	ENSP00000386635.2:n.5709+38G>T
ENST00000409709.7:c.5856+38G>T	ENSP00000386331.3:n.5856+38G>T
ENST00000458169.2:c.3282+38G>T	ENSP00000417017.2:n.3282+38G>T
ENST00000458637.6:c.5742+38G>T	ENSP00000392185.2:n.5742+38G>T
ENST00000481328.7:n.3392+38G>T
ENST00000605744.1:n.770+38G>T
NM_000260.3:c.5856+38G>T	NP_000251.3:n.5856+38G>T
NM_001127180.1:c.5742+38G>T	NP_001120652.1:n.5742+38G>T
XM_005274012.2:c.5739+38G>T	XP_005274069.1:n.5739+38G>T
XM_006718558.2:c.5847+38G>T	XP_006718621.1:n.5847+38G>T
XM_006718559.2:c.5742+38G>T	XP_006718622.1:n.5742+38G>T
XM_006718560.2:c.5739+38G>T	XP_006718623.1:n.5739+38G>T
XM_006718561.2:c.5742+38G>T	XP_006718624.1:n.5742+38G>T
XM_011545044.1:c.5856+38G>T	XP_011543346.1:n.5856+38G>T
XM_011545045.1:c.5850+38G>T	XP_011543347.1:n.5850+38G>T
XM_011545046.1:c.5823+38G>T	XP_011543348.1:n.5823+38G>T
XM_011545047.1:c.5760+38G>T	XP_011543349.1:n.5760+38G>T
XM_011545048.1:c.5631+38G>T	XP_011543350.1:n.5631+38G>T
XM_011545049.1:c.5619+38G>T	XP_011543351.1:n.5619+38G>T
XM_011545050.1:c.5592+38G>T	XP_011543352.1:n.5592+38G>T
XM_011545051.1:c.5856+38G>T	XP_011543353.1:n.5856+38G>T
XR_949938.1:n.6176+38G>T
XR_949941.1:n.6176+38G>T
XM_011545044.2:c.5856+38G>T	XP_011543346.1:n.5856+38G>T
XM_011545046.2:c.5946+38G>T	XP_011543348.2:n.5946+38G>T
XM_011545050.2:c.5592+38G>T	XP_011543352.1:n.5592+38G>T
XM_017017778.1:c.5940+38G>T	XP_016873267.1:n.5940+38G>T
XM_017017779.1:c.5937+38G>T	XP_016873268.1:n.5937+38G>T
XM_017017780.1:c.5946+38G>T	XP_016873269.1:n.5946+38G>T
XM_017017781.1:c.5850+38G>T	XP_016873270.1:n.5850+38G>T
XM_017017782.1:c.5832+38G>T	XP_016873271.1:n.5832+38G>T
XM_017017783.1:c.5829+38G>T	XP_016873272.1:n.5829+38G>T
XM_017017784.1:c.5829+38G>T	XP_016873273.1:n.5829+38G>T
XM_017017785.1:c.5709+38G>T	XP_016873274.1:n.5709+38G>T
XM_017017786.1:c.5946+38G>T	XP_016873275.1:n.5946+38G>T
XM_017017788.1:c.5832+38G>T	XP_016873277.1:n.5832+38G>T
XR_001747885.1:n.5961+38G>T
XR_001747886.1:n.5876+38G>T
XR_001747887.1:n.5947+38G>T
NM_000260.4:c.5856+38G>T MANE Select	NP_000251.3:n.5856+38G>T
NM_001127180.2:c.5742+38G>T	NP_001120652.1:n.5742+38G>T
NM_001369365.1:c.5709+38G>T	NP_001356294.1:n.5709+38G>T