Canonical Allele Identifier: CA498430503

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18049317G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18146003G>C , CM000679.2:g.18146003G>C	GRCh38
NC_000017.10:g.18049317G>C , CM000679.1:g.18049317G>C	GRCh37
NC_000017.9:g.17990042G>C	NCBI36
NG_011634.1:g.42298G>C
NG_011634.2:g.42298G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6405G>C MANE Select	ENSP00000495481.1:p.Val2135=
ENST00000205890.9:c.6405G>C	ENSP00000205890.5:p.Val2135=
ENST00000615845.4:c.6405G>C	ENSP00000481642.1:p.Val2135=
NM_016239.3:c.6405G>C	NP_057323.3:p.Val2135=
XM_011523917.1:c.6345G>C	XP_011522219.1:p.Val2115=
XM_011523918.1:c.6342+3G>C	XP_011522220.1:n.6342+3G>C
XM_011523921.1:c.6399G>C	XP_011522223.1:p.Val2133=
XR_934037.1:n.7004G>C
XR_934038.1:n.7004G>C
XM_011523918.2:c.6342+3G>C	XP_011522220.1:n.6342+3G>C
XM_017024714.2:c.6345G>C	XP_016880203.1:p.Val2115=
XM_017024715.2:c.6408G>C	XP_016880204.1:p.Val2136=
XM_024450781.1:c.6213+1411G>C	XP_024306549.1:n.6213+1411G>C
NM_016239.4:c.6405G>C MANE Select	NP_057323.3:p.Val2135=