Canonical Allele Identifier: CA498430490

Gene: MYO15A

Linked Data

• COSMIC: COSM118656
• MyVariant Identifiers: chr17:g.18049299A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18145985A>T , CM000679.2:g.18145985A>T	GRCh38
NC_000017.10:g.18049299A>T , CM000679.1:g.18049299A>T	GRCh37
NC_000017.9:g.17990024A>T	NCBI36
NG_011634.1:g.42280A>T
NG_011634.2:g.42280A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6387A>T MANE Select	ENSP00000495481.1:p.Ala2129=
ENST00000205890.9:c.6387A>T	ENSP00000205890.5:p.Ala2129=
ENST00000615845.4:c.6387A>T	ENSP00000481642.1:p.Ala2129=
NM_016239.3:c.6387A>T	NP_057323.3:p.Ala2129=
XM_011523917.1:c.6327A>T	XP_011522219.1:p.Ala2109=
XM_011523918.1:c.6327A>T	XP_011522220.1:p.Ala2109=
XM_011523921.1:c.6381A>T	XP_011522223.1:p.Ala2127=
XR_934037.1:n.6986A>T
XR_934038.1:n.6986A>T
XM_011523918.2:c.6327A>T	XP_011522220.1:p.Ala2109=
XM_017024714.2:c.6327A>T	XP_016880203.1:p.Ala2109=
XM_017024715.2:c.6390A>T	XP_016880204.1:p.Ala2130=
XM_024450781.1:c.6213+1393A>T	XP_024306549.1:n.6213+1393A>T
NM_016239.4:c.6387A>T MANE Select	NP_057323.3:p.Ala2129=