Canonical Allele Identifier: CA381950852

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76910759C>G (hg19) ; chr11:g.77199714C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77199714C>G , CM000673.2:g.77199714C>G	GRCh38
NC_000011.9:g.76910759C>G , CM000673.1:g.76910759C>G	GRCh37
NC_000011.8:g.76588407C>G	NCBI36
NG_009086.1:g.76450C>G
NG_009086.2:g.76469C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.4748C>G MANE Select	ENSP00000386331.3:p.Thr1583Ser
ENST00000670577.1:c.2589C>G
ENST00000409619.6:c.4601C>G	ENSP00000386635.2:p.Thr1534Ser
ENST00000409709.7:c.4748C>G	ENSP00000386331.3:p.Thr1583Ser
ENST00000458169.2:c.2177C>G	ENSP00000417017.2:p.Thr726Ser
ENST00000458637.6:c.4634C>G	ENSP00000392185.2:p.Thr1545Ser
ENST00000481328.7:n.2287C>G
NM_000260.3:c.4748C>G	NP_000251.3:p.Thr1583Ser
NM_001127180.1:c.4634C>G	NP_001120652.1:p.Thr1545Ser
XM_005274012.2:c.4634C>G	XP_005274069.1:p.Thr1545Ser
XM_006718558.2:c.4742C>G	XP_006718621.1:p.Thr1581Ser
XM_006718559.2:c.4634C>G	XP_006718622.1:p.Thr1545Ser
XM_006718560.2:c.4634C>G	XP_006718623.1:p.Thr1545Ser
XM_006718561.2:c.4634C>G	XP_006718624.1:p.Thr1545Ser
XM_011545044.1:c.4748C>G	XP_011543346.1:p.Thr1583Ser
XM_011545045.1:c.4742C>G	XP_011543347.1:p.Thr1581Ser
XM_011545046.1:c.4715C>G	XP_011543348.1:p.Thr1572Ser
XM_011545047.1:c.4652C>G	XP_011543349.1:p.Thr1551Ser
XM_011545048.1:c.4523C>G	XP_011543350.1:p.Thr1508Ser
XM_011545049.1:c.4511C>G	XP_011543351.1:p.Thr1504Ser
XM_011545050.1:c.4484C>G	XP_011543352.1:p.Thr1495Ser
XM_011545051.1:c.4748C>G	XP_011543353.1:p.Thr1583Ser
XM_011545052.1:c.4748C>G	XP_011543354.1:p.Thr1583Ser
XR_949938.1:n.5068C>G
XR_949941.1:n.5068C>G
XR_949942.1:n.5070C>G
XM_011545044.2:c.4748C>G	XP_011543346.1:p.Thr1583Ser
XM_011545046.2:c.4838C>G	XP_011543348.2:p.Thr1613Ser
XM_011545050.2:c.4484C>G	XP_011543352.1:p.Thr1495Ser
XM_017017778.1:c.4832C>G	XP_016873267.1:p.Thr1611Ser
XM_017017779.1:c.4832C>G	XP_016873268.1:p.Thr1611Ser
XM_017017780.1:c.4838C>G	XP_016873269.1:p.Thr1613Ser
XM_017017781.1:c.4742C>G	XP_016873270.1:p.Thr1581Ser
XM_017017782.1:c.4724C>G	XP_016873271.1:p.Thr1575Ser
XM_017017783.1:c.4724C>G	XP_016873272.1:p.Thr1575Ser
XM_017017784.1:c.4724C>G	XP_016873273.1:p.Thr1575Ser
XM_017017785.1:c.4601C>G	XP_016873274.1:p.Thr1534Ser
XM_017017786.1:c.4838C>G	XP_016873275.1:p.Thr1613Ser
XM_017017788.1:c.4724C>G	XP_016873277.1:p.Thr1575Ser
XR_001747885.1:n.4853C>G
XR_001747886.1:n.4853C>G
XR_001747887.1:n.4853C>G
XR_001747888.1:n.4853C>G
NM_000260.4:c.4748C>G MANE Select	NP_000251.3:p.Thr1583Ser
NM_001127180.2:c.4634C>G	NP_001120652.1:p.Thr1545Ser
NM_001369365.1:c.4601C>G	NP_001356294.1:p.Thr1534Ser