Canonical Allele Identifier: CA398606767
Gene: MYO15A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.18049297G>T (hg19) chr17:g.18145983G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18145983G>T , CM000679.2:g.18145983G>T GRCh38
NC_000017.10:g.18049297G>T , CM000679.1:g.18049297G>T GRCh37
NC_000017.9:g.17990022G>T NCBI36
NG_011634.1:g.42278G>T
NG_011634.2:g.42278G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6385G>T MANE Select ENSP00000495481.1:p.Ala2129Ser
ENST00000205890.9:c.6385G>T ENSP00000205890.5:p.Ala2129Ser
ENST00000615845.4:c.6385G>T ENSP00000481642.1:p.Ala2129Ser
NM_016239.3:c.6385G>T NP_057323.3:p.Ala2129Ser
XM_011523917.1:c.6325G>T XP_011522219.1:p.Ala2109Ser
XM_011523918.1:c.6325G>T XP_011522220.1:p.Ala2109Ser
XM_011523921.1:c.6379G>T XP_011522223.1:p.Ala2127Ser
XR_934037.1:n.6984G>T
XR_934038.1:n.6984G>T
XM_011523918.2:c.6325G>T XP_011522220.1:p.Ala2109Ser
XM_017024714.2:c.6325G>T XP_016880203.1:p.Ala2109Ser
XM_017024715.2:c.6388G>T XP_016880204.1:p.Ala2130Ser
XM_024450781.1:c.6213+1391G>T XP_024306549.1:n.6213+1391G>T
NM_016239.4:c.6385G>T MANE Select NP_057323.3:p.Ala2129Ser
Search 100 bp 5'
Search 100 bp 3'