Canonical Allele Identifier: CA398606669

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18049274C>A (hg19) ; chr17:g.18145960C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18145960C>A , CM000679.2:g.18145960C>A	GRCh38
NC_000017.10:g.18049274C>A , CM000679.1:g.18049274C>A	GRCh37
NC_000017.9:g.17989999C>A	NCBI36
NG_011634.1:g.42255C>A
NG_011634.2:g.42255C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6362C>A MANE Select	ENSP00000495481.1:p.Pro2121His
ENST00000205890.9:c.6362C>A	ENSP00000205890.5:p.Pro2121His
ENST00000615845.4:c.6362C>A	ENSP00000481642.1:p.Pro2121His
NM_016239.3:c.6362C>A	NP_057323.3:p.Pro2121His
XM_011523917.1:c.6302C>A	XP_011522219.1:p.Pro2101His
XM_011523918.1:c.6302C>A	XP_011522220.1:p.Pro2101His
XM_011523921.1:c.6356C>A	XP_011522223.1:p.Pro2119His
XR_934037.1:n.6961C>A
XR_934038.1:n.6961C>A
XM_011523918.2:c.6302C>A	XP_011522220.1:p.Pro2101His
XM_017024714.2:c.6302C>A	XP_016880203.1:p.Pro2101His
XM_017024715.2:c.6365C>A	XP_016880204.1:p.Pro2122His
XM_024450781.1:c.6213+1368C>A	XP_024306549.1:n.6213+1368C>A
NM_016239.4:c.6362C>A MANE Select	NP_057323.3:p.Pro2121His