Canonical Allele Identifier: CA398597558

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18041516T>G (hg19) ; chr17:g.18138202T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18138202T>G , CM000679.2:g.18138202T>G	GRCh38
NC_000017.10:g.18041516T>G , CM000679.1:g.18041516T>G	GRCh37
NC_000017.9:g.17982241T>G	NCBI36
NG_011634.1:g.34497T>G
NG_011634.2:g.34497T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646238.1:n.227T>G
ENST00000647165.2:c.4963T>G MANE Select	ENSP00000495481.1:p.Tyr1655Asp
ENST00000205890.9:c.4963T>G	ENSP00000205890.5:p.Tyr1655Asp
ENST00000615845.4:c.4963T>G	ENSP00000481642.1:p.Tyr1655Asp
NM_016239.3:c.4963T>G	NP_057323.3:p.Tyr1655Asp
XM_011523917.1:c.4957T>G	XP_011522219.1:p.Tyr1653Asp
XM_011523918.1:c.4957T>G	XP_011522220.1:p.Tyr1653Asp
XM_011523919.1:c.4957T>G	XP_011522221.1:p.Tyr1653Asp
XM_011523920.1:c.4957T>G	XP_011522222.1:p.Tyr1653Asp
XM_011523921.1:c.4957T>G	XP_011522223.1:p.Tyr1653Asp
XR_934037.1:n.5616T>G
XR_934038.1:n.5616T>G
XR_934039.1:n.5616T>G
XM_011523918.2:c.4957T>G	XP_011522220.1:p.Tyr1653Asp
XM_017024714.2:c.4957T>G	XP_016880203.1:p.Tyr1653Asp
XM_017024715.2:c.4966T>G	XP_016880204.1:p.Tyr1656Asp
XM_024450780.1:c.4957T>G	XP_024306548.1:p.Tyr1653Asp
XM_024450781.1:c.4957T>G	XP_024306549.1:p.Tyr1653Asp
XM_024450782.1:c.4957T>G	XP_024306550.1:p.Tyr1653Asp
XR_934039.2:n.5655T>G
NM_016239.4:c.4963T>G MANE Select	NP_057323.3:p.Tyr1655Asp