Canonical Allele Identifier: CA2250851754

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18149430_18149431delinsTG , CM000679.2:g.18149430_18149431delinsTG	GRCh38
NC_000017.10:g.18052744_18052745delinsTG , CM000679.1:g.18052744_18052745delinsTG	GRCh37
NC_000017.9:g.17993469_17993470delinsTG	NCBI36
NG_011634.1:g.45725_45726delinsTG
NG_011634.2:g.45725_45726delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7117+54_7118-55delinsTG MANE Select	ENSP00000495481.1:n.7117+54_7118-55delinsTG
ENST00000205890.9:c.7117+54_7118-55delinsTG	ENSP00000205890.5:n.7117+54_7118-55delinsTG
ENST00000578999.1:n.683_684delinsTG
ENST00000615845.4:c.7117+54_7118-55delinsTG	ENSP00000481642.1:n.7117+54_7118-55delinsTG
NM_016239.3:c.7117+54_7118-55delinsTG	NP_057323.3:n.7117+54_7118-55delinsTG
XM_011523917.1:c.6792+54_6793-55delinsTG	XP_011522219.1:n.6792+54_6793-55delinsTG
XM_011523921.1:c.7111+54_7112-55delinsTG	XP_011522223.1:n.7111+54_7112-55delinsTG
XR_934037.1:n.7451+54_7452-55delinsTG
XR_934038.1:n.7404-56_7404-55delinsTG
XR_934293.1:n.435-1825_435-1824delinsCA
XR_934295.1:n.254-1825_254-1824delinsCA
XM_017024714.2:c.7057+54_7058-55delinsTG	XP_016880203.1:n.7057+54_7058-55delinsTG
XM_017024715.2:c.7120+54_7121-55delinsTG	XP_016880204.1:n.7120+54_7121-55delinsTG
XR_934293.2:n.378-1825_378-1824delinsCA
NM_016239.4:c.7117+54_7118-55delinsTG MANE Select	NP_057323.3:n.7117+54_7118-55delinsTG