Canonical Allele Identifier: CA256879921

Gene: MYO16

Linked Data

• dbSNP Id: rs7984522
• gnomAD v2: 13-109347659-T-A
• gnomAD v3: 13-108695311-T-A
• gnomAD v4: 13-108695311-T-A
• MyVariant Identifiers: chr13:g.109347659T>A (hg19) ; chr13:g.108695311T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108695311T>A , CM000675.2:g.108695311T>A	GRCh38
NC_000013.10:g.109347659T>A , CM000675.1:g.109347659T>A	GRCh37
NC_000013.9:g.108145660T>A	NCBI36
NG_053147.1:g.204583T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251041.10:c.227-17350T>A	ENSP00000251041.5:n.227-17350T>A
ENST00000356711.7:c.227-17350T>A	ENSP00000349145.2:n.227-17350T>A
ENST00000457511.7:c.293-17350T>A MANE Select	ENSP00000401633.3:n.293-17350T>A
ENST00000251041.9:c.227-17350T>A	ENSP00000251041.5:n.227-17350T>A
ENST00000356711.6:c.227-17350T>A	ENSP00000349145.2:n.227-17350T>A
ENST00000357550.3:c.227-17350T>A	ENSP00000350160.2:n.227-17350T>A
ENST00000457511.6:c.293-17350T>A	ENSP00000401633.3:n.293-17350T>A
NM_001198950.1:c.293-17350T>A	NP_001185879.1:n.293-17350T>A
NM_015011.1:c.227-17350T>A	NP_055826.1:n.227-17350T>A
XM_011521062.1:c.227-17350T>A	XP_011519364.1:n.227-17350T>A
NM_001198950.2:c.293-17350T>A	NP_001185879.1:n.293-17350T>A
NM_015011.2:c.227-17350T>A	NP_055826.1:n.227-17350T>A
NM_001198950.3:c.293-17350T>A MANE Select	NP_001185879.1:n.293-17350T>A
NM_015011.3:c.227-17350T>A	NP_055826.1:n.227-17350T>A