Canonical Allele Identifier: CA398607017
Gene: MYO15A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.18049340A>C (hg19) chr17:g.18146026A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146026A>C , CM000679.2:g.18146026A>C GRCh38
NC_000017.10:g.18049340A>C , CM000679.1:g.18049340A>C GRCh37
NC_000017.9:g.17990065A>C NCBI36
NG_011634.1:g.42321A>C
NG_011634.2:g.42321A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6428A>C MANE Select ENSP00000495481.1:p.Asn2143Thr
ENST00000205890.9:c.6428A>C ENSP00000205890.5:p.Asn2143Thr
ENST00000578999.1:n.13A>C
ENST00000615845.4:c.6428A>C ENSP00000481642.1:p.Asn2143Thr
NM_016239.3:c.6428A>C NP_057323.3:p.Asn2143Thr
XM_011523917.1:c.6368A>C XP_011522219.1:p.Asn2123Thr
XM_011523918.1:c.6342+26A>C XP_011522220.1:n.6342+26A>C
XM_011523921.1:c.6422A>C XP_011522223.1:p.Asn2141Thr
XR_934037.1:n.7027A>C
XR_934038.1:n.7027A>C
XM_011523918.2:c.6342+26A>C XP_011522220.1:n.6342+26A>C
XM_017024714.2:c.6368A>C XP_016880203.1:p.Asn2123Thr
XM_017024715.2:c.6431A>C XP_016880204.1:p.Asn2144Thr
XM_024450781.1:c.6213+1434A>C XP_024306549.1:n.6213+1434A>C
NM_016239.4:c.6428A>C MANE Select NP_057323.3:p.Asn2143Thr
Search 100 bp 5'
Search 100 bp 3'