Canonical Allele Identifier: CA398633933

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18062629G>C (hg19) ; chr17:g.18159315G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159315G>C , CM000679.2:g.18159315G>C	GRCh38
NC_000017.10:g.18062629G>C , CM000679.1:g.18062629G>C	GRCh37
NC_000017.9:g.18003354G>C	NCBI36
NG_011634.1:g.55610G>C
NG_011634.2:g.55610G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1535G>C
ENST00000643693.1:n.999G>C
ENST00000644795.1:c.989G>C	ENSP00000495720.1:p.Ser330Thr
ENST00000646782.1:n.1931G>C
ENST00000647165.2:c.9197G>C MANE Select	ENSP00000495481.1:p.Ser3066Thr
ENST00000651214.1:n.1702G>C
ENST00000205890.9:c.9197G>C	ENSP00000205890.5:p.Ser3066Thr
ENST00000418233.7:c.989G>C	ENSP00000408800.3:p.Ser330Thr
ENST00000433411.7:n.134G>C
ENST00000445289.6:n.316+1415G>C
ENST00000556535.5:c.59G>C	ENSP00000451782.1:p.Ser20Thr
ENST00000557190.5:n.99G>C
ENST00000557655.5:c.59G>C	ENSP00000451925.1:p.Ser20Thr
ENST00000578472.5:c.59G>C	ENSP00000467989.1:p.Ser20Thr
ENST00000615845.4:c.9197G>C	ENSP00000481642.1:p.Ser3066Thr
NM_016239.3:c.9197G>C	NP_057323.3:p.Ser3066Thr
XM_011523921.1:c.9191G>C	XP_011522223.1:p.Ser3064Thr
XM_017024714.2:c.9137G>C	XP_016880203.1:p.Ser3046Thr
XM_017024715.2:c.9200G>C	XP_016880204.1:p.Ser3067Thr
NM_016239.4:c.9197G>C MANE Select	NP_057323.3:p.Ser3066Thr