Canonical Allele Identifier: CA381950959

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76910810G>T (hg19) ; chr11:g.77199765G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77199765G>T , CM000673.2:g.77199765G>T	GRCh38
NC_000011.9:g.76910810G>T , CM000673.1:g.76910810G>T	GRCh37
NC_000011.8:g.76588458G>T	NCBI36
NG_009086.1:g.76501G>T
NG_009086.2:g.76520G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.4799G>T MANE Select	ENSP00000386331.3:p.Gly1600Val
ENST00000670577.1:c.2640G>T
ENST00000409619.6:c.4652G>T	ENSP00000386635.2:p.Gly1551Val
ENST00000409709.7:c.4799G>T	ENSP00000386331.3:p.Gly1600Val
ENST00000458169.2:c.2228G>T	ENSP00000417017.2:p.Gly743Val
ENST00000458637.6:c.4685G>T	ENSP00000392185.2:p.Gly1562Val
ENST00000481328.7:n.2338G>T
NM_000260.3:c.4799G>T	NP_000251.3:p.Gly1600Val
NM_001127180.1:c.4685G>T	NP_001120652.1:p.Gly1562Val
XM_005274012.2:c.4685G>T	XP_005274069.1:p.Gly1562Val
XM_006718558.2:c.4793G>T	XP_006718621.1:p.Gly1598Val
XM_006718559.2:c.4685G>T	XP_006718622.1:p.Gly1562Val
XM_006718560.2:c.4685G>T	XP_006718623.1:p.Gly1562Val
XM_006718561.2:c.4685G>T	XP_006718624.1:p.Gly1562Val
XM_011545044.1:c.4799G>T	XP_011543346.1:p.Gly1600Val
XM_011545045.1:c.4793G>T	XP_011543347.1:p.Gly1598Val
XM_011545046.1:c.4766G>T	XP_011543348.1:p.Gly1589Val
XM_011545047.1:c.4703G>T	XP_011543349.1:p.Gly1568Val
XM_011545048.1:c.4574G>T	XP_011543350.1:p.Gly1525Val
XM_011545049.1:c.4562G>T	XP_011543351.1:p.Gly1521Val
XM_011545050.1:c.4535G>T	XP_011543352.1:p.Gly1512Val
XM_011545051.1:c.4799G>T	XP_011543353.1:p.Gly1600Val
XM_011545052.1:c.4799G>T	XP_011543354.1:p.Gly1600Val
XR_949938.1:n.5119G>T
XR_949941.1:n.5119G>T
XR_949942.1:n.5121G>T
XM_011545044.2:c.4799G>T	XP_011543346.1:p.Gly1600Val
XM_011545046.2:c.4889G>T	XP_011543348.2:p.Gly1630Val
XM_011545050.2:c.4535G>T	XP_011543352.1:p.Gly1512Val
XM_017017778.1:c.4883G>T	XP_016873267.1:p.Gly1628Val
XM_017017779.1:c.4883G>T	XP_016873268.1:p.Gly1628Val
XM_017017780.1:c.4889G>T	XP_016873269.1:p.Gly1630Val
XM_017017781.1:c.4793G>T	XP_016873270.1:p.Gly1598Val
XM_017017782.1:c.4775G>T	XP_016873271.1:p.Gly1592Val
XM_017017783.1:c.4775G>T	XP_016873272.1:p.Gly1592Val
XM_017017784.1:c.4775G>T	XP_016873273.1:p.Gly1592Val
XM_017017785.1:c.4652G>T	XP_016873274.1:p.Gly1551Val
XM_017017786.1:c.4889G>T	XP_016873275.1:p.Gly1630Val
XM_017017788.1:c.4775G>T	XP_016873277.1:p.Gly1592Val
XR_001747885.1:n.4904G>T
XR_001747886.1:n.4904G>T
XR_001747887.1:n.4904G>T
XR_001747888.1:n.4904G>T
NM_000260.4:c.4799G>T MANE Select	NP_000251.3:p.Gly1600Val
NM_001127180.2:c.4685G>T	NP_001120652.1:p.Gly1562Val
NM_001369365.1:c.4652G>T	NP_001356294.1:p.Gly1551Val