Canonical Allele Identifier: CA2615254078

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77179178-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77179178_77179179insTC , CM000673.2:g.77179178_77179179insTC	GRCh38
NC_000011.9:g.76890224_76890225insTC , CM000673.1:g.76890224_76890225insTC	GRCh37
NC_000011.8:g.76567872_76567873insTC	NCBI36
NG_009086.1:g.55915_55916insTC
NG_009086.2:g.55933_55934insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.2367+49_2367+50insTC MANE Select	ENSP00000386331.3:n.2367+49_2367+50insTC
ENST00000409893.6:c.432+49_432+50insTC	ENSP00000386689.2:n.432+49_432+50insTC
ENST00000670577.1:c.208+49_208+50insTC
ENST00000409619.6:c.2334+49_2334+50insTC	ENSP00000386635.2:n.2334+49_2334+50insTC
ENST00000409709.7:c.2367+49_2367+50insTC	ENSP00000386331.3:n.2367+49_2367+50insTC
ENST00000409893.5:c.2367+49_2367+50insTC	ENSP00000386689.1:n.2367+49_2367+50insTC
ENST00000458637.6:c.2367+49_2367+50insTC	ENSP00000392185.2:n.2367+49_2367+50insTC
ENST00000620575.4:c.2367+49_2367+50insTC	ENSP00000477640.1:n.2367+49_2367+50insTC
NM_000260.3:c.2367+49_2367+50insTC	NP_000251.3:n.2367+49_2367+50insTC
NM_001127179.2:c.2367+49_2367+50insTC	NP_001120651.2:n.2367+49_2367+50insTC
NM_001127180.1:c.2367+49_2367+50insTC	NP_001120652.1:n.2367+49_2367+50insTC
XM_005274012.2:c.2367+49_2367+50insTC	XP_005274069.1:n.2367+49_2367+50insTC
XM_006718558.2:c.2367+49_2367+50insTC	XP_006718621.1:n.2367+49_2367+50insTC
XM_006718559.2:c.2367+49_2367+50insTC	XP_006718622.1:n.2367+49_2367+50insTC
XM_006718560.2:c.2367+49_2367+50insTC	XP_006718623.1:n.2367+49_2367+50insTC
XM_006718561.2:c.2367+49_2367+50insTC	XP_006718624.1:n.2367+49_2367+50insTC
XM_011545044.1:c.2367+49_2367+50insTC	XP_011543346.1:n.2367+49_2367+50insTC
XM_011545045.1:c.2367+49_2367+50insTC	XP_011543347.1:n.2367+49_2367+50insTC
XM_011545046.1:c.2334+49_2334+50insTC	XP_011543348.1:n.2334+49_2334+50insTC
XM_011545047.1:c.2367+49_2367+50insTC	XP_011543349.1:n.2367+49_2367+50insTC
XM_011545048.1:c.2367+49_2367+50insTC	XP_011543350.1:n.2367+49_2367+50insTC
XM_011545049.1:c.2136+49_2136+50insTC	XP_011543351.1:n.2136+49_2136+50insTC
XM_011545050.1:c.2109+49_2109+50insTC	XP_011543352.1:n.2109+49_2109+50insTC
XM_011545051.1:c.2367+49_2367+50insTC	XP_011543353.1:n.2367+49_2367+50insTC
XM_011545052.1:c.2367+49_2367+50insTC	XP_011543354.1:n.2367+49_2367+50insTC
XR_949938.1:n.2687+49_2687+50insTC
XR_949941.1:n.2687+49_2687+50insTC
XR_949942.1:n.2689+49_2689+50insTC
XR_949943.1:n.2689+49_2689+50insTC
XM_011545044.2:c.2367+49_2367+50insTC	XP_011543346.1:n.2367+49_2367+50insTC
XM_011545046.2:c.2457+49_2457+50insTC	XP_011543348.2:n.2457+49_2457+50insTC
XM_011545050.2:c.2109+49_2109+50insTC	XP_011543352.1:n.2109+49_2109+50insTC
XM_017017778.1:c.2457+49_2457+50insTC	XP_016873267.1:n.2457+49_2457+50insTC
XM_017017779.1:c.2457+49_2457+50insTC	XP_016873268.1:n.2457+49_2457+50insTC
XM_017017780.1:c.2457+49_2457+50insTC	XP_016873269.1:n.2457+49_2457+50insTC
XM_017017781.1:c.2457+49_2457+50insTC	XP_016873270.1:n.2457+49_2457+50insTC
XM_017017782.1:c.2457+49_2457+50insTC	XP_016873271.1:n.2457+49_2457+50insTC
XM_017017783.1:c.2457+49_2457+50insTC	XP_016873272.1:n.2457+49_2457+50insTC
XM_017017784.1:c.2457+49_2457+50insTC	XP_016873273.1:n.2457+49_2457+50insTC
XM_017017785.1:c.2226+49_2226+50insTC	XP_016873274.1:n.2226+49_2226+50insTC
XM_017017786.1:c.2457+49_2457+50insTC	XP_016873275.1:n.2457+49_2457+50insTC
XM_017017787.1:c.2457+49_2457+50insTC	XP_016873276.1:n.2457+49_2457+50insTC
XM_017017788.1:c.2457+49_2457+50insTC	XP_016873277.1:n.2457+49_2457+50insTC
XR_001747885.1:n.2472+49_2472+50insTC
XR_001747886.1:n.2472+49_2472+50insTC
XR_001747887.1:n.2472+49_2472+50insTC
XR_001747888.1:n.2472+49_2472+50insTC
XR_001747889.1:n.2472+49_2472+50insTC
NM_000260.4:c.2367+49_2367+50insTC MANE Select	NP_000251.3:n.2367+49_2367+50insTC
NM_001127180.2:c.2367+49_2367+50insTC	NP_001120652.1:n.2367+49_2367+50insTC
NM_001369365.1:c.2334+49_2334+50insTC	NP_001356294.1:n.2334+49_2334+50insTC