Canonical Allele Identifier: CA1984128653

Gene: MYO7A

Linked Data

• dbSNP Id: rs1957662765

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77208843A>G , CM000673.2:g.77208843A>G	GRCh38
NC_000011.9:g.76919888A>G , CM000673.1:g.76919888A>G	GRCh37
NC_000011.8:g.76597536A>G	NCBI36
NG_009086.1:g.85579A>G
NG_009086.2:g.85598A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6051+40A>G MANE Select	ENSP00000386331.3:n.6051+40A>G
ENST00000670577.1:c.3852+40A>G
ENST00000409619.6:c.5904+40A>G	ENSP00000386635.2:n.5904+40A>G
ENST00000409709.7:c.6051+40A>G	ENSP00000386331.3:n.6051+40A>G
ENST00000458169.2:c.3477+40A>G	ENSP00000417017.2:n.3477+40A>G
ENST00000458637.6:c.5937+40A>G	ENSP00000392185.2:n.5937+40A>G
ENST00000481328.7:n.3587+40A>G
ENST00000605744.1:n.1005A>G
NM_000260.3:c.6051+40A>G	NP_000251.3:n.6051+40A>G
NM_001127180.1:c.5937+40A>G	NP_001120652.1:n.5937+40A>G
XM_005274012.2:c.5934+40A>G	XP_005274069.1:n.5934+40A>G
XM_006718558.2:c.6042+40A>G	XP_006718621.1:n.6042+40A>G
XM_006718559.2:c.5937+40A>G	XP_006718622.1:n.5937+40A>G
XM_006718560.2:c.5934+40A>G	XP_006718623.1:n.5934+40A>G
XM_006718561.2:c.5937+40A>G	XP_006718624.1:n.5937+40A>G
XM_011545044.1:c.6051+40A>G	XP_011543346.1:n.6051+40A>G
XM_011545045.1:c.6045+40A>G	XP_011543347.1:n.6045+40A>G
XM_011545046.1:c.6018+40A>G	XP_011543348.1:n.6018+40A>G
XM_011545047.1:c.5955+40A>G	XP_011543349.1:n.5955+40A>G
XM_011545048.1:c.5826+40A>G	XP_011543350.1:n.5826+40A>G
XM_011545049.1:c.5814+40A>G	XP_011543351.1:n.5814+40A>G
XM_011545050.1:c.5787+40A>G	XP_011543352.1:n.5787+40A>G
XM_011545051.1:c.6051+40A>G	XP_011543353.1:n.6051+40A>G
XR_949938.1:n.6371+40A>G
XR_949941.1:n.6345+40A>G
XM_011545044.2:c.6051+40A>G	XP_011543346.1:n.6051+40A>G
XM_011545046.2:c.6141+40A>G	XP_011543348.2:n.6141+40A>G
XM_011545050.2:c.5787+40A>G	XP_011543352.1:n.5787+40A>G
XM_017017778.1:c.6135+40A>G	XP_016873267.1:n.6135+40A>G
XM_017017779.1:c.6132+40A>G	XP_016873268.1:n.6132+40A>G
XM_017017780.1:c.6141+40A>G	XP_016873269.1:n.6141+40A>G
XM_017017781.1:c.6045+40A>G	XP_016873270.1:n.6045+40A>G
XM_017017782.1:c.6027+40A>G	XP_016873271.1:n.6027+40A>G
XM_017017783.1:c.6024+40A>G	XP_016873272.1:n.6024+40A>G
XM_017017784.1:c.6024+40A>G	XP_016873273.1:n.6024+40A>G
XM_017017785.1:c.5904+40A>G	XP_016873274.1:n.5904+40A>G
XM_017017786.1:c.6141+40A>G	XP_016873275.1:n.6141+40A>G
XM_017017788.1:c.6027+40A>G	XP_016873277.1:n.6027+40A>G
XR_001747885.1:n.6130+40A>G
XR_001747886.1:n.6071+40A>G
XR_001747887.1:n.6116+40A>G
NM_000260.4:c.6051+40A>G MANE Select	NP_000251.3:n.6051+40A>G
NM_001127180.2:c.5937+40A>G	NP_001120652.1:n.5937+40A>G
NM_001369365.1:c.5904+40A>G	NP_001356294.1:n.5904+40A>G