Canonical Allele Identifier: CA398633990

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18062635G>A (hg19) ; chr17:g.18159321G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159321G>A , CM000679.2:g.18159321G>A	GRCh38
NC_000017.10:g.18062635G>A , CM000679.1:g.18062635G>A	GRCh37
NC_000017.9:g.18003360G>A	NCBI36
NG_011634.1:g.55616G>A
NG_011634.2:g.55616G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1541G>A
ENST00000643693.1:n.1005G>A
ENST00000644795.1:c.995G>A	ENSP00000495720.1:p.Ser332Asn
ENST00000646782.1:n.1937G>A
ENST00000647165.2:c.9203G>A MANE Select	ENSP00000495481.1:p.Ser3068Asn
ENST00000651214.1:n.1708G>A
ENST00000205890.9:c.9203G>A	ENSP00000205890.5:p.Ser3068Asn
ENST00000418233.7:c.995G>A	ENSP00000408800.3:p.Ser332Asn
ENST00000433411.7:n.140G>A
ENST00000445289.6:n.316+1421G>A
ENST00000556535.5:c.65G>A	ENSP00000451782.1:p.Ser22Asn
ENST00000557190.5:n.105G>A
ENST00000557655.5:c.65G>A	ENSP00000451925.1:p.Ser22Asn
ENST00000578472.5:c.65G>A	ENSP00000467989.1:p.Ser22Asn
ENST00000615845.4:c.9203G>A	ENSP00000481642.1:p.Ser3068Asn
NM_016239.3:c.9203G>A	NP_057323.3:p.Ser3068Asn
XM_011523921.1:c.9197G>A	XP_011522223.1:p.Ser3066Asn
XM_017024714.2:c.9143G>A	XP_016880203.1:p.Ser3048Asn
XM_017024715.2:c.9206G>A	XP_016880204.1:p.Ser3069Asn
NM_016239.4:c.9203G>A MANE Select	NP_057323.3:p.Ser3068Asn