Canonical Allele Identifier: CA381951014

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76910839G>A (hg19) ; chr11:g.77199794G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77199794G>A , CM000673.2:g.77199794G>A	GRCh38
NC_000011.9:g.76910839G>A , CM000673.1:g.76910839G>A	GRCh37
NC_000011.8:g.76588487G>A	NCBI36
NG_009086.1:g.76530G>A
NG_009086.2:g.76549G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.4828G>A MANE Select	ENSP00000386331.3:p.Ala1610Thr
ENST00000670577.1:c.2669G>A
ENST00000409619.6:c.4681G>A	ENSP00000386635.2:p.Ala1561Thr
ENST00000409709.7:c.4828G>A	ENSP00000386331.3:p.Ala1610Thr
ENST00000458169.2:c.2257G>A	ENSP00000417017.2:p.Ala753Thr
ENST00000458637.6:c.4714G>A	ENSP00000392185.2:p.Ala1572Thr
ENST00000481328.7:n.2367G>A
NM_000260.3:c.4828G>A	NP_000251.3:p.Ala1610Thr
NM_001127180.1:c.4714G>A	NP_001120652.1:p.Ala1572Thr
XM_005274012.2:c.4714G>A	XP_005274069.1:p.Ala1572Thr
XM_006718558.2:c.4822G>A	XP_006718621.1:p.Ala1608Thr
XM_006718559.2:c.4714G>A	XP_006718622.1:p.Ala1572Thr
XM_006718560.2:c.4714G>A	XP_006718623.1:p.Ala1572Thr
XM_006718561.2:c.4714G>A	XP_006718624.1:p.Ala1572Thr
XM_011545044.1:c.4828G>A	XP_011543346.1:p.Ala1610Thr
XM_011545045.1:c.4822G>A	XP_011543347.1:p.Ala1608Thr
XM_011545046.1:c.4795G>A	XP_011543348.1:p.Ala1599Thr
XM_011545047.1:c.4732G>A	XP_011543349.1:p.Ala1578Thr
XM_011545048.1:c.4603G>A	XP_011543350.1:p.Ala1535Thr
XM_011545049.1:c.4591G>A	XP_011543351.1:p.Ala1531Thr
XM_011545050.1:c.4564G>A	XP_011543352.1:p.Ala1522Thr
XM_011545051.1:c.4828G>A	XP_011543353.1:p.Ala1610Thr
XM_011545052.1:c.4828G>A	XP_011543354.1:p.Ala1610Thr
XR_949938.1:n.5148G>A
XR_949941.1:n.5148G>A
XR_949942.1:n.5150G>A
XM_011545044.2:c.4828G>A	XP_011543346.1:p.Ala1610Thr
XM_011545046.2:c.4918G>A	XP_011543348.2:p.Ala1640Thr
XM_011545050.2:c.4564G>A	XP_011543352.1:p.Ala1522Thr
XM_017017778.1:c.4912G>A	XP_016873267.1:p.Ala1638Thr
XM_017017779.1:c.4912G>A	XP_016873268.1:p.Ala1638Thr
XM_017017780.1:c.4918G>A	XP_016873269.1:p.Ala1640Thr
XM_017017781.1:c.4822G>A	XP_016873270.1:p.Ala1608Thr
XM_017017782.1:c.4804G>A	XP_016873271.1:p.Ala1602Thr
XM_017017783.1:c.4804G>A	XP_016873272.1:p.Ala1602Thr
XM_017017784.1:c.4804G>A	XP_016873273.1:p.Ala1602Thr
XM_017017785.1:c.4681G>A	XP_016873274.1:p.Ala1561Thr
XM_017017786.1:c.4918G>A	XP_016873275.1:p.Ala1640Thr
XM_017017788.1:c.4804G>A	XP_016873277.1:p.Ala1602Thr
XR_001747885.1:n.4933G>A
XR_001747886.1:n.4933G>A
XR_001747887.1:n.4933G>A
XR_001747888.1:n.4933G>A
NM_000260.4:c.4828G>A MANE Select	NP_000251.3:p.Ala1610Thr
NM_001127180.2:c.4714G>A	NP_001120652.1:p.Ala1572Thr
NM_001369365.1:c.4681G>A	NP_001356294.1:p.Ala1561Thr