Canonical Allele Identifier: CA2615269377

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77214738-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214738C>A , CM000673.2:g.77214738C>A	GRCh38
NC_000011.9:g.76925783C>A , CM000673.1:g.76925783C>A	GRCh37
NC_000011.8:g.76603431C>A	NCBI36
NG_009086.1:g.91474C>A
NG_009086.2:g.91493C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.*42C>A MANE Select	ENSP00000386331.3:n.*42C>A
ENST00000670577.1:c.4491C>A
ENST00000409619.6:c.*42C>A	ENSP00000386635.2:n.*42C>A
ENST00000409709.7:c.*42C>A	ENSP00000386331.3:n.*42C>A
ENST00000458169.2:c.4116C>A	ENSP00000417017.2:n.4116C>A
ENST00000458637.6:c.*42C>A	ENSP00000392185.2:n.*42C>A
ENST00000481328.7:n.5240C>A
ENST00000605744.1:n.2204C>A
NM_000260.3:c.*42C>A	NP_000251.3:n.*42C>A
NM_001127180.1:c.*42C>A	NP_001120652.1:n.*42C>A
XM_005274012.2:c.*42C>A	XP_005274069.1:n.*42C>A
XM_006718561.2:c.*42C>A	XP_006718624.1:n.*42C>A
XR_949941.1:n.6984C>A
XM_017017780.1:c.*42C>A	XP_016873269.1:n.*42C>A
XM_017017784.1:c.*42C>A	XP_016873273.1:n.*42C>A
XM_017017788.1:c.*42C>A	XP_016873277.1:n.*42C>A
XR_001747885.1:n.6769C>A
XR_001747887.1:n.6755C>A
NM_000260.4:c.*42C>A MANE Select	NP_000251.3:n.*42C>A
NM_001127180.2:c.*42C>A	NP_001120652.1:n.*42C>A
NM_001369365.1:c.*42C>A	NP_001356294.1:n.*42C>A