Canonical Allele Identifier: CA2615250910

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77158324-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77158324_77158325insTG , CM000673.2:g.77158324_77158325insTG	GRCh38
NC_000011.9:g.76869370_76869371insTG , CM000673.1:g.76869370_76869371insTG	GRCh37
NC_000011.8:g.76547018_76547019insTG	NCBI36
NG_009086.1:g.35061_35062insTG
NG_009086.2:g.35079_35080insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.897_898insTG MANE Select	ENSP00000386331.3:p.Asn300Ter
ENST00000409619.6:c.864_865insTG	ENSP00000386635.2:p.Asn289Ter
ENST00000409709.7:c.897_898insTG	ENSP00000386331.3:p.Asn300Ter
ENST00000409893.5:c.897_898insTG	ENSP00000386689.1:p.Asn300Ter
ENST00000458637.6:c.897_898insTG	ENSP00000392185.2:p.Asn300Ter
ENST00000620575.4:c.897_898insTG	ENSP00000477640.1:p.Asn300Ter
NM_000260.3:c.897_898insTG	NP_000251.3:p.Asn300Ter
NM_001127179.2:c.897_898insTG	NP_001120651.2:p.Asn300Ter
NM_001127180.1:c.897_898insTG	NP_001120652.1:p.Asn300Ter
XM_005274012.2:c.897_898insTG	XP_005274069.1:p.Asn300Ter
XM_006718558.2:c.897_898insTG	XP_006718621.1:p.Asn300Ter
XM_006718559.2:c.897_898insTG	XP_006718622.1:p.Asn300Ter
XM_006718560.2:c.897_898insTG	XP_006718623.1:p.Asn300Ter
XM_006718561.2:c.897_898insTG	XP_006718624.1:p.Asn300Ter
XM_011545044.1:c.897_898insTG	XP_011543346.1:p.Asn300Ter
XM_011545045.1:c.897_898insTG	XP_011543347.1:p.Asn300Ter
XM_011545046.1:c.864_865insTG	XP_011543348.1:p.Asn289Ter
XM_011545047.1:c.897_898insTG	XP_011543349.1:p.Asn300Ter
XM_011545048.1:c.897_898insTG	XP_011543350.1:p.Asn300Ter
XM_011545049.1:c.849+932_849+933insTG	XP_011543351.1:n.849+932_849+933insTG
XM_011545050.1:c.639_640insTG	XP_011543352.1:p.Asn214Ter
XM_011545051.1:c.897_898insTG	XP_011543353.1:p.Asn300Ter
XM_011545052.1:c.897_898insTG	XP_011543354.1:p.Asn300Ter
XR_949938.1:n.1217_1218insTG
XR_949941.1:n.1217_1218insTG
XR_949942.1:n.1219_1220insTG
XR_949943.1:n.1219_1220insTG
XM_011545044.2:c.897_898insTG	XP_011543346.1:p.Asn300Ter
XM_011545046.2:c.987_988insTG	XP_011543348.2:p.Asn330Ter
XM_011545050.2:c.639_640insTG	XP_011543352.1:p.Asn214Ter
XM_017017778.1:c.987_988insTG	XP_016873267.1:p.Asn330Ter
XM_017017779.1:c.987_988insTG	XP_016873268.1:p.Asn330Ter
XM_017017780.1:c.987_988insTG	XP_016873269.1:p.Asn330Ter
XM_017017781.1:c.987_988insTG	XP_016873270.1:p.Asn330Ter
XM_017017782.1:c.987_988insTG	XP_016873271.1:p.Asn330Ter
XM_017017783.1:c.987_988insTG	XP_016873272.1:p.Asn330Ter
XM_017017784.1:c.987_988insTG	XP_016873273.1:p.Asn330Ter
XM_017017785.1:c.939+932_939+933insTG	XP_016873274.1:n.939+932_939+933insTG
XM_017017786.1:c.987_988insTG	XP_016873275.1:p.Asn330Ter
XM_017017787.1:c.987_988insTG	XP_016873276.1:p.Asn330Ter
XM_017017788.1:c.987_988insTG	XP_016873277.1:p.Asn330Ter
XR_001747885.1:n.1002_1003insTG
XR_001747886.1:n.1002_1003insTG
XR_001747887.1:n.1002_1003insTG
XR_001747888.1:n.1002_1003insTG
XR_001747889.1:n.1002_1003insTG
NM_000260.4:c.897_898insTG MANE Select	NP_000251.3:p.Asn300Ter
NM_001127180.2:c.897_898insTG	NP_001120652.1:p.Asn300Ter
NM_001369365.1:c.864_865insTG	NP_001356294.1:p.Asn289Ter