Canonical Allele Identifier: CA381950911

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77199743-C-A
• MyVariant Identifiers: chr11:g.76910788C>A (hg19) ; chr11:g.77199743C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77199743C>A , CM000673.2:g.77199743C>A	GRCh38
NC_000011.9:g.76910788C>A , CM000673.1:g.76910788C>A	GRCh37
NC_000011.8:g.76588436C>A	NCBI36
NG_009086.1:g.76479C>A
NG_009086.2:g.76498C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.4777C>A MANE Select	ENSP00000386331.3:p.Leu1593Met
ENST00000670577.1:c.2618C>A
ENST00000409619.6:c.4630C>A	ENSP00000386635.2:p.Leu1544Met
ENST00000409709.7:c.4777C>A	ENSP00000386331.3:p.Leu1593Met
ENST00000458169.2:c.2206C>A	ENSP00000417017.2:p.Leu736Met
ENST00000458637.6:c.4663C>A	ENSP00000392185.2:p.Leu1555Met
ENST00000481328.7:n.2316C>A
NM_000260.3:c.4777C>A	NP_000251.3:p.Leu1593Met
NM_001127180.1:c.4663C>A	NP_001120652.1:p.Leu1555Met
XM_005274012.2:c.4663C>A	XP_005274069.1:p.Leu1555Met
XM_006718558.2:c.4771C>A	XP_006718621.1:p.Leu1591Met
XM_006718559.2:c.4663C>A	XP_006718622.1:p.Leu1555Met
XM_006718560.2:c.4663C>A	XP_006718623.1:p.Leu1555Met
XM_006718561.2:c.4663C>A	XP_006718624.1:p.Leu1555Met
XM_011545044.1:c.4777C>A	XP_011543346.1:p.Leu1593Met
XM_011545045.1:c.4771C>A	XP_011543347.1:p.Leu1591Met
XM_011545046.1:c.4744C>A	XP_011543348.1:p.Leu1582Met
XM_011545047.1:c.4681C>A	XP_011543349.1:p.Leu1561Met
XM_011545048.1:c.4552C>A	XP_011543350.1:p.Leu1518Met
XM_011545049.1:c.4540C>A	XP_011543351.1:p.Leu1514Met
XM_011545050.1:c.4513C>A	XP_011543352.1:p.Leu1505Met
XM_011545051.1:c.4777C>A	XP_011543353.1:p.Leu1593Met
XM_011545052.1:c.4777C>A	XP_011543354.1:p.Leu1593Met
XR_949938.1:n.5097C>A
XR_949941.1:n.5097C>A
XR_949942.1:n.5099C>A
XM_011545044.2:c.4777C>A	XP_011543346.1:p.Leu1593Met
XM_011545046.2:c.4867C>A	XP_011543348.2:p.Leu1623Met
XM_011545050.2:c.4513C>A	XP_011543352.1:p.Leu1505Met
XM_017017778.1:c.4861C>A	XP_016873267.1:p.Leu1621Met
XM_017017779.1:c.4861C>A	XP_016873268.1:p.Leu1621Met
XM_017017780.1:c.4867C>A	XP_016873269.1:p.Leu1623Met
XM_017017781.1:c.4771C>A	XP_016873270.1:p.Leu1591Met
XM_017017782.1:c.4753C>A	XP_016873271.1:p.Leu1585Met
XM_017017783.1:c.4753C>A	XP_016873272.1:p.Leu1585Met
XM_017017784.1:c.4753C>A	XP_016873273.1:p.Leu1585Met
XM_017017785.1:c.4630C>A	XP_016873274.1:p.Leu1544Met
XM_017017786.1:c.4867C>A	XP_016873275.1:p.Leu1623Met
XM_017017788.1:c.4753C>A	XP_016873277.1:p.Leu1585Met
XR_001747885.1:n.4882C>A
XR_001747886.1:n.4882C>A
XR_001747887.1:n.4882C>A
XR_001747888.1:n.4882C>A
NM_000260.4:c.4777C>A MANE Select	NP_000251.3:p.Leu1593Met
NM_001127180.2:c.4663C>A	NP_001120652.1:p.Leu1555Met
NM_001369365.1:c.4630C>A	NP_001356294.1:p.Leu1544Met