Canonical Allele Identifier: CA381953816

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77207288-G-T
• MyVariant Identifiers: chr11:g.76918333G>T (hg19) ; chr11:g.77207288G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77207288G>T , CM000673.2:g.77207288G>T	GRCh38
NC_000011.9:g.76918333G>T , CM000673.1:g.76918333G>T	GRCh37
NC_000011.8:g.76595981G>T	NCBI36
NG_009086.1:g.84024G>T
NG_009086.2:g.84043G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.5743-1G>T MANE Select	ENSP00000386331.3:n.5743-1G>T
ENST00000670577.1:c.3570-1G>T
ENST00000409619.6:c.5596-1G>T	ENSP00000386635.2:n.5596-1G>T
ENST00000409709.7:c.5743-1G>T	ENSP00000386331.3:n.5743-1G>T
ENST00000458169.2:c.3169-1G>T	ENSP00000417017.2:n.3169-1G>T
ENST00000458637.6:c.5629-1G>T	ENSP00000392185.2:n.5629-1G>T
ENST00000481328.7:n.3279-1G>T
ENST00000605744.1:n.656G>T
NM_000260.3:c.5743-1G>T	NP_000251.3:n.5743-1G>T
NM_001127180.1:c.5629-1G>T	NP_001120652.1:n.5629-1G>T
XM_005274012.2:c.5626-1G>T	XP_005274069.1:n.5626-1G>T
XM_006718558.2:c.5734-1G>T	XP_006718621.1:n.5734-1G>T
XM_006718559.2:c.5629-1G>T	XP_006718622.1:n.5629-1G>T
XM_006718560.2:c.5626-1G>T	XP_006718623.1:n.5626-1G>T
XM_006718561.2:c.5629-1G>T	XP_006718624.1:n.5629-1G>T
XM_011545044.1:c.5743-1G>T	XP_011543346.1:n.5743-1G>T
XM_011545045.1:c.5737-1G>T	XP_011543347.1:n.5737-1G>T
XM_011545046.1:c.5710-1G>T	XP_011543348.1:n.5710-1G>T
XM_011545047.1:c.5647-1G>T	XP_011543349.1:n.5647-1G>T
XM_011545048.1:c.5518-1G>T	XP_011543350.1:n.5518-1G>T
XM_011545049.1:c.5506-1G>T	XP_011543351.1:n.5506-1G>T
XM_011545050.1:c.5479-1G>T	XP_011543352.1:n.5479-1G>T
XM_011545051.1:c.5743-1G>T	XP_011543353.1:n.5743-1G>T
XR_949938.1:n.6063-1G>T
XR_949941.1:n.6063-1G>T
XM_011545044.2:c.5743-1G>T	XP_011543346.1:n.5743-1G>T
XM_011545046.2:c.5833-1G>T	XP_011543348.2:n.5833-1G>T
XM_011545050.2:c.5479-1G>T	XP_011543352.1:n.5479-1G>T
XM_017017778.1:c.5827-1G>T	XP_016873267.1:n.5827-1G>T
XM_017017779.1:c.5824-1G>T	XP_016873268.1:n.5824-1G>T
XM_017017780.1:c.5833-1G>T	XP_016873269.1:n.5833-1G>T
XM_017017781.1:c.5737-1G>T	XP_016873270.1:n.5737-1G>T
XM_017017782.1:c.5719-1G>T	XP_016873271.1:n.5719-1G>T
XM_017017783.1:c.5716-1G>T	XP_016873272.1:n.5716-1G>T
XM_017017784.1:c.5716-1G>T	XP_016873273.1:n.5716-1G>T
XM_017017785.1:c.5596-1G>T	XP_016873274.1:n.5596-1G>T
XM_017017786.1:c.5833-1G>T	XP_016873275.1:n.5833-1G>T
XM_017017788.1:c.5719-1G>T	XP_016873277.1:n.5719-1G>T
XR_001747885.1:n.5848-1G>T
XR_001747886.1:n.5763-1G>T
XR_001747887.1:n.5834-1G>T
NM_000260.4:c.5743-1G>T MANE Select	NP_000251.3:n.5743-1G>T
NM_001127180.2:c.5629-1G>T	NP_001120652.1:n.5629-1G>T
NM_001369365.1:c.5596-1G>T	NP_001356294.1:n.5596-1G>T