Canonical Allele Identifier: CA381950878

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76910771C>G (hg19) ; chr11:g.77199726C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77199726C>G , CM000673.2:g.77199726C>G	GRCh38
NC_000011.9:g.76910771C>G , CM000673.1:g.76910771C>G	GRCh37
NC_000011.8:g.76588419C>G	NCBI36
NG_009086.1:g.76462C>G
NG_009086.2:g.76481C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.4760C>G MANE Select	ENSP00000386331.3:p.Ala1587Gly
ENST00000670577.1:c.2601C>G
ENST00000409619.6:c.4613C>G	ENSP00000386635.2:p.Ala1538Gly
ENST00000409709.7:c.4760C>G	ENSP00000386331.3:p.Ala1587Gly
ENST00000458169.2:c.2189C>G	ENSP00000417017.2:p.Ala730Gly
ENST00000458637.6:c.4646C>G	ENSP00000392185.2:p.Ala1549Gly
ENST00000481328.7:n.2299C>G
NM_000260.3:c.4760C>G	NP_000251.3:p.Ala1587Gly
NM_001127180.1:c.4646C>G	NP_001120652.1:p.Ala1549Gly
XM_005274012.2:c.4646C>G	XP_005274069.1:p.Ala1549Gly
XM_006718558.2:c.4754C>G	XP_006718621.1:p.Ala1585Gly
XM_006718559.2:c.4646C>G	XP_006718622.1:p.Ala1549Gly
XM_006718560.2:c.4646C>G	XP_006718623.1:p.Ala1549Gly
XM_006718561.2:c.4646C>G	XP_006718624.1:p.Ala1549Gly
XM_011545044.1:c.4760C>G	XP_011543346.1:p.Ala1587Gly
XM_011545045.1:c.4754C>G	XP_011543347.1:p.Ala1585Gly
XM_011545046.1:c.4727C>G	XP_011543348.1:p.Ala1576Gly
XM_011545047.1:c.4664C>G	XP_011543349.1:p.Ala1555Gly
XM_011545048.1:c.4535C>G	XP_011543350.1:p.Ala1512Gly
XM_011545049.1:c.4523C>G	XP_011543351.1:p.Ala1508Gly
XM_011545050.1:c.4496C>G	XP_011543352.1:p.Ala1499Gly
XM_011545051.1:c.4760C>G	XP_011543353.1:p.Ala1587Gly
XM_011545052.1:c.4760C>G	XP_011543354.1:p.Ala1587Gly
XR_949938.1:n.5080C>G
XR_949941.1:n.5080C>G
XR_949942.1:n.5082C>G
XM_011545044.2:c.4760C>G	XP_011543346.1:p.Ala1587Gly
XM_011545046.2:c.4850C>G	XP_011543348.2:p.Ala1617Gly
XM_011545050.2:c.4496C>G	XP_011543352.1:p.Ala1499Gly
XM_017017778.1:c.4844C>G	XP_016873267.1:p.Ala1615Gly
XM_017017779.1:c.4844C>G	XP_016873268.1:p.Ala1615Gly
XM_017017780.1:c.4850C>G	XP_016873269.1:p.Ala1617Gly
XM_017017781.1:c.4754C>G	XP_016873270.1:p.Ala1585Gly
XM_017017782.1:c.4736C>G	XP_016873271.1:p.Ala1579Gly
XM_017017783.1:c.4736C>G	XP_016873272.1:p.Ala1579Gly
XM_017017784.1:c.4736C>G	XP_016873273.1:p.Ala1579Gly
XM_017017785.1:c.4613C>G	XP_016873274.1:p.Ala1538Gly
XM_017017786.1:c.4850C>G	XP_016873275.1:p.Ala1617Gly
XM_017017788.1:c.4736C>G	XP_016873277.1:p.Ala1579Gly
XR_001747885.1:n.4865C>G
XR_001747886.1:n.4865C>G
XR_001747887.1:n.4865C>G
XR_001747888.1:n.4865C>G
NM_000260.4:c.4760C>G MANE Select	NP_000251.3:p.Ala1587Gly
NM_001127180.2:c.4646C>G	NP_001120652.1:p.Ala1549Gly
NM_001369365.1:c.4613C>G	NP_001356294.1:p.Ala1538Gly