Canonical Allele Identifier: CA2792789129

Gene: MYO7A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214723_77214724insACA , CM000673.2:g.77214723_77214724insACA	GRCh38
NC_000011.9:g.76925768_76925769insACA , CM000673.1:g.76925768_76925769insACA	GRCh37
NC_000011.8:g.76603416_76603417insACA	NCBI36
NG_009086.1:g.91459_91460insACA
NG_009086.2:g.91478_91479insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.*27_*28insACA MANE Select	ENSP00000386331.3:n.*27_*28insACA
ENST00000670577.1:c.4476_4477insACA
ENST00000409619.6:c.*27_*28insACA	ENSP00000386635.2:n.*27_*28insACA
ENST00000409709.7:c.*27_*28insACA	ENSP00000386331.3:n.*27_*28insACA
ENST00000458169.2:c.4101_4102insACA	ENSP00000417017.2:n.4101_4102insACA
ENST00000458637.6:c.*27_*28insACA	ENSP00000392185.2:n.*27_*28insACA
ENST00000481328.7:n.5225_5226insACA
ENST00000605744.1:n.2189_2190insACA
NM_000260.3:c.*27_*28insACA	NP_000251.3:n.*27_*28insACA
NM_001127180.1:c.*27_*28insACA	NP_001120652.1:n.*27_*28insACA
XM_005274012.2:c.*27_*28insACA	XP_005274069.1:n.*27_*28insACA
XM_006718561.2:c.*27_*28insACA	XP_006718624.1:n.*27_*28insACA
XR_949941.1:n.6969_6970insACA
XM_017017780.1:c.*27_*28insACA	XP_016873269.1:n.*27_*28insACA
XM_017017784.1:c.*27_*28insACA	XP_016873273.1:n.*27_*28insACA
XM_017017788.1:c.*27_*28insACA	XP_016873277.1:n.*27_*28insACA
XR_001747885.1:n.6754_6755insACA
XR_001747887.1:n.6740_6741insACA
NM_000260.4:c.*27_*28insACA MANE Select	NP_000251.3:n.*27_*28insACA
NM_001127180.2:c.*27_*28insACA	NP_001120652.1:n.*27_*28insACA
NM_001369365.1:c.*27_*28insACA	NP_001356294.1:n.*27_*28insACA