Canonical Allele Identifier: CA726662682

Gene: MYO15A

Linked Data

• dbSNP Id: rs1277130024
• gnomAD v3: 17-18159235-T-C
• gnomAD v4: 17-18159235-T-C
• MyVariant Identifiers: chr17:g.18062549T>C (hg19) ; chr17:g.18159235T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159235T>C , CM000679.2:g.18159235T>C	GRCh38
NC_000017.10:g.18062549T>C , CM000679.1:g.18062549T>C	GRCh37
NC_000017.9:g.18003274T>C	NCBI36
NG_011634.1:g.55530T>C
NG_011634.2:g.55530T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1495-40T>C
ENST00000643693.1:n.959-40T>C
ENST00000644795.1:c.949-40T>C	ENSP00000495720.1:n.949-40T>C
ENST00000646782.1:n.1891-40T>C
ENST00000647165.2:c.9157-40T>C MANE Select	ENSP00000495481.1:n.9157-40T>C
ENST00000651214.1:n.1662-40T>C
ENST00000205890.9:c.9157-40T>C	ENSP00000205890.5:n.9157-40T>C
ENST00000418233.7:c.949-40T>C	ENSP00000408800.3:n.949-40T>C
ENST00000433411.7:n.94-40T>C
ENST00000445289.6:n.316+1335T>C
ENST00000556535.5:c.19-40T>C	ENSP00000451782.1:n.19-40T>C
ENST00000557190.5:n.59-40T>C
ENST00000557655.5:c.19-40T>C	ENSP00000451925.1:n.19-40T>C
ENST00000578472.5:c.19-40T>C	ENSP00000467989.1:n.19-40T>C
ENST00000615845.4:c.9157-40T>C	ENSP00000481642.1:n.9157-40T>C
NM_016239.3:c.9157-40T>C	NP_057323.3:n.9157-40T>C
XM_011523921.1:c.9151-40T>C	XP_011522223.1:n.9151-40T>C
XM_017024714.2:c.9097-40T>C	XP_016880203.1:n.9097-40T>C
XM_017024715.2:c.9160-40T>C	XP_016880204.1:n.9160-40T>C
NM_016239.4:c.9157-40T>C MANE Select	NP_057323.3:n.9157-40T>C