Canonical Allele Identifier: CA8424944
Community Standard Title: NM_016239.4(MYO15A):c.7787+27G>T
Gene: MYO15A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18151554G>T , CM000679.2:g.18151554G>T GRCh38
NC_000017.10:g.18054868G>T , CM000679.1:g.18054868G>T GRCh37
NC_000017.9:g.17995593G>T NCBI36
NG_011634.1:g.47849G>T
NG_011634.2:g.47849G>T

Transcript Alleles

HGVS Amino-acid Change
NM_016239.4:c.7787+27G>T MANE Select NP_057323.3:n.7787+27G>T
ENST00000647165.2:c.7787+27G>T MANE Select ENSP00000495481.1:n.7787+27G>T
NM_016239.3:c.7787+27G>T NP_057323.3:n.7787+27G>T
ENST00000205890.9:c.7787+27G>T ENSP00000205890.5:n.7787+27G>T
ENST00000615845.4:c.7787+27G>T ENSP00000481642.1:n.7787+27G>T
XM_011523921.1:c.7781+27G>T XP_011522223.1:n.7781+27G>T
XM_017024714.2:c.7727+27G>T XP_016880203.1:n.7727+27G>T
XM_017024715.2:c.7790+27G>T XP_016880204.1:n.7790+27G>T
XR_934293.1:n.434+49C>A
XR_934293.2:n.377+49C>A
XR_934294.1:n.434+49C>A
XR_934294.2:n.377+49C>A
XR_934295.1:n.253+49C>A