Canonical Allele Identifier: CA2615263287

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77211335-CGGGTGAGCATG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211341_77211351del , CM000673.2:g.77211341_77211351del	GRCh38
NC_000011.9:g.76922386_76922396del , CM000673.1:g.76922386_76922396del	GRCh37
NC_000011.8:g.76600034_76600044del	NCBI36
NG_009086.1:g.88077_88087del
NG_009086.2:g.88096_88106del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6237+4_6237+14del
ENST00000670577.1:c.4038+4_4038+14del
ENST00000409619.6:c.6090+4_6090+14del
ENST00000409709.7:c.6237+4_6237+14del
ENST00000458169.2:c.3663+4_3663+14del
ENST00000458637.6:c.6123+4_6123+14del
ENST00000481328.7:n.3773+4_3773+14del
ENST00000526863.2:n.25+430_25+440del
ENST00000605744.1:n.1704+4_1704+14del
NM_000260.3:c.6237+4_6237+14del
NM_001127180.1:c.6123+4_6123+14del
XM_005274012.2:c.6120+4_6120+14del
XM_006718558.2:c.6228+4_6228+14del
XM_006718559.2:c.6123+4_6123+14del
XM_006718560.2:c.6120+4_6120+14del
XM_006718561.2:c.6123+4_6123+14del
XM_011545044.1:c.6237+4_6237+14del
XM_011545045.1:c.6231+4_6231+14del
XM_011545046.1:c.6204+4_6204+14del
XM_011545047.1:c.6141+4_6141+14del
XM_011545048.1:c.6012+4_6012+14del
XM_011545049.1:c.6000+4_6000+14del
XM_011545050.1:c.5973+4_5973+14del
XM_011545051.1:c.6237+4_6237+14del
XR_949938.1:n.6557+4_6557+14del
XR_949941.1:n.6531+4_6531+14del
XM_011545044.2:c.6237+4_6237+14del
XM_011545046.2:c.6327+4_6327+14del
XM_011545050.2:c.5973+4_5973+14del
XM_017017778.1:c.6321+4_6321+14del
XM_017017779.1:c.6318+4_6318+14del
XM_017017780.1:c.6327+4_6327+14del
XM_017017781.1:c.6231+4_6231+14del
XM_017017782.1:c.6213+4_6213+14del
XM_017017783.1:c.6210+4_6210+14del
XM_017017784.1:c.6210+4_6210+14del
XM_017017785.1:c.6090+4_6090+14del
XM_017017786.1:c.6327+4_6327+14del
XM_017017788.1:c.6213+4_6213+14del
XR_001747885.1:n.6316+4_6316+14del
XR_001747887.1:n.6302+4_6302+14del
NM_000260.4:c.6237+4_6237+14del
NM_001127180.2:c.6123+4_6123+14del
NM_001369365.1:c.6090+4_6090+14del