Canonical Allele Identifier: CA656612192

Gene: MYO15A

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18149397G>T , CM000679.2:g.18149397G>T	GRCh38
NC_000017.10:g.18052711G>T , CM000679.1:g.18052711G>T	GRCh37
NC_000017.9:g.17993436G>T	NCBI36
NG_011634.1:g.45692G>T
NG_011634.2:g.45692G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7117+21G>T MANE Select	ENSP00000495481.1:n.7117+21G>T
ENST00000205890.9:c.7117+21G>T	ENSP00000205890.5:n.7117+21G>T
ENST00000578999.1:n.650G>T
ENST00000615845.4:c.7117+21G>T	ENSP00000481642.1:n.7117+21G>T
NM_016239.3:c.7117+21G>T	NP_057323.3:n.7117+21G>T
XM_011523917.1:c.6792+21G>T	XP_011522219.1:n.6792+21G>T
XM_011523921.1:c.7111+21G>T	XP_011522223.1:n.7111+21G>T
XR_934037.1:n.7451+21G>T
XR_934038.1:n.7403+69G>T
XR_934293.1:n.435-1791C>A
XR_934295.1:n.254-1791C>A
XM_017024714.2:c.7057+21G>T	XP_016880203.1:n.7057+21G>T
XM_017024715.2:c.7120+21G>T	XP_016880204.1:n.7120+21G>T
XR_934293.2:n.378-1791C>A
NM_016239.4:c.7117+21G>T MANE Select	NP_057323.3:n.7117+21G>T