Canonical Allele Identifier: CA398606586

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18049253T>C (hg19) ; chr17:g.18145939T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18145939T>C , CM000679.2:g.18145939T>C	GRCh38
NC_000017.10:g.18049253T>C , CM000679.1:g.18049253T>C	GRCh37
NC_000017.9:g.17989978T>C	NCBI36
NG_011634.1:g.42234T>C
NG_011634.2:g.42234T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6341T>C MANE Select	ENSP00000495481.1:p.Val2114Ala
ENST00000205890.9:c.6341T>C	ENSP00000205890.5:p.Val2114Ala
ENST00000615845.4:c.6341T>C	ENSP00000481642.1:p.Val2114Ala
NM_016239.3:c.6341T>C	NP_057323.3:p.Val2114Ala
XM_011523917.1:c.6281T>C	XP_011522219.1:p.Val2094Ala
XM_011523918.1:c.6281T>C	XP_011522220.1:p.Val2094Ala
XM_011523921.1:c.6335T>C	XP_011522223.1:p.Val2112Ala
XR_934037.1:n.6940T>C
XR_934038.1:n.6940T>C
XM_011523918.2:c.6281T>C	XP_011522220.1:p.Val2094Ala
XM_017024714.2:c.6281T>C	XP_016880203.1:p.Val2094Ala
XM_017024715.2:c.6344T>C	XP_016880204.1:p.Val2115Ala
XM_024450781.1:c.6213+1347T>C	XP_024306549.1:n.6213+1347T>C
NM_016239.4:c.6341T>C MANE Select	NP_057323.3:p.Val2114Ala