Canonical Allele Identifier: CA2615254901

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77208377-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77208377C>A , CM000673.2:g.77208377C>A	GRCh38
NC_000011.9:g.76919422C>A , CM000673.1:g.76919422C>A	GRCh37
NC_000011.8:g.76597070C>A	NCBI36
NG_009086.1:g.85113C>A
NG_009086.2:g.85132C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.5857-53C>A MANE Select	ENSP00000386331.3:n.5857-53C>A
ENST00000670577.1:c.3684-53C>A
ENST00000409619.6:c.5710-53C>A	ENSP00000386635.2:n.5710-53C>A
ENST00000409709.7:c.5857-53C>A	ENSP00000386331.3:n.5857-53C>A
ENST00000458169.2:c.3283-53C>A	ENSP00000417017.2:n.3283-53C>A
ENST00000458637.6:c.5743-53C>A	ENSP00000392185.2:n.5743-53C>A
ENST00000481328.7:n.3393-53C>A
ENST00000605744.1:n.771-53C>A
NM_000260.3:c.5857-53C>A	NP_000251.3:n.5857-53C>A
NM_001127180.1:c.5743-53C>A	NP_001120652.1:n.5743-53C>A
XM_005274012.2:c.5740-53C>A	XP_005274069.1:n.5740-53C>A
XM_006718558.2:c.5848-53C>A	XP_006718621.1:n.5848-53C>A
XM_006718559.2:c.5743-53C>A	XP_006718622.1:n.5743-53C>A
XM_006718560.2:c.5740-53C>A	XP_006718623.1:n.5740-53C>A
XM_006718561.2:c.5743-53C>A	XP_006718624.1:n.5743-53C>A
XM_011545044.1:c.5857-53C>A	XP_011543346.1:n.5857-53C>A
XM_011545045.1:c.5851-53C>A	XP_011543347.1:n.5851-53C>A
XM_011545046.1:c.5824-53C>A	XP_011543348.1:n.5824-53C>A
XM_011545047.1:c.5761-53C>A	XP_011543349.1:n.5761-53C>A
XM_011545048.1:c.5632-53C>A	XP_011543350.1:n.5632-53C>A
XM_011545049.1:c.5620-53C>A	XP_011543351.1:n.5620-53C>A
XM_011545050.1:c.5593-53C>A	XP_011543352.1:n.5593-53C>A
XM_011545051.1:c.5857-53C>A	XP_011543353.1:n.5857-53C>A
XR_949938.1:n.6177-53C>A
XR_949941.1:n.6177-53C>A
XM_011545044.2:c.5857-53C>A	XP_011543346.1:n.5857-53C>A
XM_011545046.2:c.5947-53C>A	XP_011543348.2:n.5947-53C>A
XM_011545050.2:c.5593-53C>A	XP_011543352.1:n.5593-53C>A
XM_017017778.1:c.5941-53C>A	XP_016873267.1:n.5941-53C>A
XM_017017779.1:c.5938-53C>A	XP_016873268.1:n.5938-53C>A
XM_017017780.1:c.5947-53C>A	XP_016873269.1:n.5947-53C>A
XM_017017781.1:c.5851-53C>A	XP_016873270.1:n.5851-53C>A
XM_017017782.1:c.5833-53C>A	XP_016873271.1:n.5833-53C>A
XM_017017783.1:c.5830-53C>A	XP_016873272.1:n.5830-53C>A
XM_017017784.1:c.5830-53C>A	XP_016873273.1:n.5830-53C>A
XM_017017785.1:c.5710-53C>A	XP_016873274.1:n.5710-53C>A
XM_017017786.1:c.5947-53C>A	XP_016873275.1:n.5947-53C>A
XM_017017788.1:c.5833-53C>A	XP_016873277.1:n.5833-53C>A
XR_001747885.1:n.5962-53C>A
XR_001747886.1:n.5877-53C>A
XR_001747887.1:n.5948-53C>A
NM_000260.4:c.5857-53C>A MANE Select	NP_000251.3:n.5857-53C>A
NM_001127180.2:c.5743-53C>A	NP_001120652.1:n.5743-53C>A
NM_001369365.1:c.5710-53C>A	NP_001356294.1:n.5710-53C>A