Canonical Allele Identifier: CA398621464
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18151859A>G , CM000679.2:g.18151859A>G GRCh38
NC_000017.10:g.18055173A>G , CM000679.1:g.18055173A>G GRCh37
NC_000017.9:g.17995898A>G NCBI36
NG_011634.1:g.48154A>G
NG_011634.2:g.48154A>G

Transcript Alleles

HGVS Amino-acid Change
NM_016239.4:c.7801A>G MANE Select NP_057323.3:p.Lys2601Glu
ENST00000647165.2:c.7801A>G MANE Select ENSP00000495481.1:p.Lys2601Glu
NM_016239.3:c.7801A>G NP_057323.3:p.Lys2601Glu
ENST00000205890.9:c.7801A>G ENSP00000205890.5:p.Lys2601Glu
ENST00000615845.4:c.7801A>G ENSP00000481642.1:p.Lys2601Glu
XM_011523921.1:c.7795A>G XP_011522223.1:p.Lys2599Glu
XM_017024714.2:c.7741A>G XP_016880203.1:p.Lys2581Glu
XM_017024715.2:c.7804A>G XP_016880204.1:p.Lys2602Glu
XR_934293.1:n.178T>C
XR_934293.2:n.121T>C
XR_934294.1:n.178T>C
XR_934294.2:n.121T>C
XR_934295.1:n.131-134T>C