Canonical Allele Identifier: CA2250851179

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18148133C= , CM000679.2:g.18148133C=	GRCh38
NC_000017.10:g.18051447C= , CM000679.1:g.18051447C=	GRCh37
NC_000017.9:g.17992172C=	NCBI36
NG_011634.1:g.44428C=
NG_011634.2:g.44428C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6614C= MANE Select	ENSP00000495481.1:p.Thr2205=
ENST00000205890.9:c.6614C=	ENSP00000205890.5:p.Thr2205=
ENST00000578999.1:n.199C=
ENST00000615845.4:c.6614C=	ENSP00000481642.1:p.Thr2205=
NM_016239.3:c.6614C=	NP_057323.3:p.Thr2205=
XM_011523917.1:c.6554C=	XP_011522219.1:p.Thr2185=
XM_011523918.1:c.*93C=	XP_011522220.1:n.*93C=
XM_011523921.1:c.6608C=	XP_011522223.1:p.Thr2203=
XR_934037.1:n.7213C=
XR_934038.1:n.7213C=
XR_934293.1:n.435-527G=
XR_934295.1:n.254-527G=
XM_017024714.2:c.6554C=	XP_016880203.1:p.Thr2185=
XM_017024715.2:c.6617C=	XP_016880204.1:p.Thr2206=
XR_934293.2:n.378-527G=
NM_016239.4:c.6614C= MANE Select	NP_057323.3:p.Thr2205=