Canonical Allele Identifier: CA13922134

Gene: MYO16

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108728378A>C , CM000675.2:g.108728378A>C	GRCh38
NC_000013.10:g.109380726A>C , CM000675.1:g.109380726A>C	GRCh37
NC_000013.9:g.108178727A>C	NCBI36
NG_053147.1:g.237650A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251041.10:c.441+795A>C	ENSP00000251041.5:n.441+795A>C
ENST00000356711.7:c.441+795A>C	ENSP00000349145.2:n.441+795A>C
ENST00000457511.7:c.507+795A>C MANE Select	ENSP00000401633.3:n.507+795A>C
ENST00000251041.9:c.441+795A>C	ENSP00000251041.5:n.441+795A>C
ENST00000356711.6:c.441+795A>C	ENSP00000349145.2:n.441+795A>C
ENST00000357550.3:c.441+795A>C	ENSP00000350160.2:n.441+795A>C
ENST00000457511.6:c.507+795A>C	ENSP00000401633.3:n.507+795A>C
NM_001198950.1:c.507+795A>C	NP_001185879.1:n.507+795A>C
NM_015011.1:c.441+795A>C	NP_055826.1:n.441+795A>C
XM_011521062.1:c.441+795A>C	XP_011519364.1:n.441+795A>C
NM_001198950.2:c.507+795A>C	NP_001185879.1:n.507+795A>C
NM_015011.2:c.441+795A>C	NP_055826.1:n.441+795A>C
NM_001198950.3:c.507+795A>C MANE Select	NP_001185879.1:n.507+795A>C
NM_015011.3:c.441+795A>C	NP_055826.1:n.441+795A>C