Canonical Allele Identifier: CA2250851372
Community Standard Title: NM_016239.4(MYO15A):c.6764+2T=
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18148570T= , CM000679.2:g.18148570T= GRCh38
NC_000017.10:g.18051884T= , CM000679.1:g.18051884T= GRCh37
NC_000017.9:g.17992609T= NCBI36
NG_011634.1:g.44865T=
NG_011634.2:g.44865T=

Transcript Alleles

HGVS Amino-acid Change
NM_016239.4:c.6764+2T= MANE Select NP_057323.3:n.6764+2T=
ENST00000647165.2:c.6764+2T= MANE Select ENSP00000495481.1:n.6764+2T=
NM_016239.3:c.6764+2T= NP_057323.3:n.6764+2T=
ENST00000205890.9:c.6764+2T= ENSP00000205890.5:n.6764+2T=
ENST00000578999.1:n.277-191T=
ENST00000615845.4:c.6764+2T= ENSP00000481642.1:n.6764+2T=
XM_011523917.1:c.6631+360T= XP_011522219.1:n.6631+360T=
XM_011523921.1:c.6758+2T= XP_011522223.1:n.6758+2T=
XM_017024714.2:c.6704+2T= XP_016880203.1:n.6704+2T=
XM_017024715.2:c.6767+2T= XP_016880204.1:n.6767+2T=
XR_934037.1:n.7290+360T=
XR_934038.1:n.7290+360T=
XR_934293.1:n.435-964A=
XR_934293.2:n.378-964A=
XR_934295.1:n.254-964A=