Canonical Allele Identifier: CA2615269328
Gene: MYO7A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.77214707G>C , CM000673.2:g.77214707G>C GRCh38
NC_000011.9:g.76925752G>C , CM000673.1:g.76925752G>C GRCh37
NC_000011.8:g.76603400G>C NCBI36
NG_009086.1:g.91443G>C
NG_009086.2:g.91462G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000409709.9:c.*11G>C MANE Select ENSP00000386331.3:n.*11G>C
ENST00000670577.1:c.4460G>C
ENST00000409619.6:c.*11G>C ENSP00000386635.2:n.*11G>C
ENST00000409709.7:c.*11G>C ENSP00000386331.3:n.*11G>C
ENST00000458169.2:c.4085G>C ENSP00000417017.2:n.4085G>C
ENST00000458637.6:c.*11G>C ENSP00000392185.2:n.*11G>C
ENST00000481328.7:n.5209G>C
ENST00000605744.1:n.2173G>C
NM_000260.3:c.*11G>C NP_000251.3:n.*11G>C
NM_001127180.1:c.*11G>C NP_001120652.1:n.*11G>C
XM_005274012.2:c.*11G>C XP_005274069.1:n.*11G>C
XM_006718561.2:c.*11G>C XP_006718624.1:n.*11G>C
XR_949941.1:n.6953G>C
XM_017017780.1:c.*11G>C XP_016873269.1:n.*11G>C
XM_017017784.1:c.*11G>C XP_016873273.1:n.*11G>C
XM_017017788.1:c.*11G>C XP_016873277.1:n.*11G>C
XR_001747885.1:n.6738G>C
XR_001747887.1:n.6724G>C
NM_000260.4:c.*11G>C MANE Select NP_000251.3:n.*11G>C
NM_001127180.2:c.*11G>C NP_001120652.1:n.*11G>C
NM_001369365.1:c.*11G>C NP_001356294.1:n.*11G>C