Canonical Allele Identifier: CA498430493

Gene: MYO15A

Linked Data

• dbSNP Id: rs2046472916
• MyVariant Identifiers: chr17:g.18049303C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18145989C>T , CM000679.2:g.18145989C>T	GRCh38
NC_000017.10:g.18049303C>T , CM000679.1:g.18049303C>T	GRCh37
NC_000017.9:g.17990028C>T	NCBI36
NG_011634.1:g.42284C>T
NG_011634.2:g.42284C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6391C>T MANE Select	ENSP00000495481.1:p.Leu2131=
ENST00000205890.9:c.6391C>T	ENSP00000205890.5:p.Leu2131=
ENST00000615845.4:c.6391C>T	ENSP00000481642.1:p.Leu2131=
NM_016239.3:c.6391C>T	NP_057323.3:p.Leu2131=
XM_011523917.1:c.6331C>T	XP_011522219.1:p.Leu2111=
XM_011523918.1:c.6331C>T	XP_011522220.1:p.Leu2111=
XM_011523921.1:c.6385C>T	XP_011522223.1:p.Leu2129=
XR_934037.1:n.6990C>T
XR_934038.1:n.6990C>T
XM_011523918.2:c.6331C>T	XP_011522220.1:p.Leu2111=
XM_017024714.2:c.6331C>T	XP_016880203.1:p.Leu2111=
XM_017024715.2:c.6394C>T	XP_016880204.1:p.Leu2132=
XM_024450781.1:c.6213+1397C>T	XP_024306549.1:n.6213+1397C>T
NM_016239.4:c.6391C>T MANE Select	NP_057323.3:p.Leu2131=