Canonical Allele Identifier: CA132440

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214596C>T , CM000673.2:g.77214596C>T	GRCh38
NC_000011.9:g.76925641C>T , CM000673.1:g.76925641C>T	GRCh37
NC_000011.8:g.76603289C>T	NCBI36
NG_009086.1:g.91332C>T
NG_009086.2:g.91351C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6559-11C>T MANE Select	ENSP00000386331.3:n.6559-11C>T
ENST00000670577.1:c.4360-11C>T
ENST00000409619.6:c.6412-11C>T	ENSP00000386635.2:n.6412-11C>T
ENST00000409709.7:c.6559-11C>T	ENSP00000386331.3:n.6559-11C>T
ENST00000458169.2:c.3985-11C>T	ENSP00000417017.2:n.3985-11C>T
ENST00000458637.6:c.6439-11C>T	ENSP00000392185.2:n.6439-11C>T
ENST00000481328.7:n.5109-11C>T
ENST00000605744.1:n.2073-11C>T
NM_000260.3:c.6559-11C>T	NP_000251.3:n.6559-11C>T
NM_001127180.1:c.6439-11C>T	NP_001120652.1:n.6439-11C>T
XM_005274012.2:c.6442-11C>T	XP_005274069.1:n.6442-11C>T
XM_006718561.2:c.6445-11C>T	XP_006718624.1:n.6445-11C>T
XR_949941.1:n.6853-11C>T
XM_017017780.1:c.6649-11C>T	XP_016873269.1:n.6649-11C>T
XM_017017784.1:c.6532-11C>T	XP_016873273.1:n.6532-11C>T
XM_017017788.1:c.6535-11C>T	XP_016873277.1:n.6535-11C>T
XR_001747885.1:n.6638-11C>T
XR_001747887.1:n.6624-11C>T
NM_000260.4:c.6559-11C>T MANE Select	NP_000251.3:n.6559-11C>T
NM_001127180.2:c.6439-11C>T	NP_001120652.1:n.6439-11C>T
NM_001369365.1:c.6412-11C>T	NP_001356294.1:n.6412-11C>T