Canonical Allele Identifier: CA13838353

Gene: MYO16

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108803487G>A , CM000675.2:g.108803487G>A	GRCh38
NC_000013.10:g.109455835G>A , CM000675.1:g.109455835G>A	GRCh37
NC_000013.9:g.108253836G>A	NCBI36
NG_053147.1:g.312759G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251041.10:c.676-3192G>A	ENSP00000251041.5:n.676-3192G>A
ENST00000356711.7:c.676-3192G>A	ENSP00000349145.2:n.676-3192G>A
ENST00000457511.7:c.742-3192G>A MANE Select	ENSP00000401633.3:n.742-3192G>A
ENST00000251041.9:c.676-3192G>A	ENSP00000251041.5:n.676-3192G>A
ENST00000356711.6:c.676-3192G>A	ENSP00000349145.2:n.676-3192G>A
ENST00000357550.3:c.676-3192G>A	ENSP00000350160.2:n.676-3192G>A
ENST00000375857.6:n.62-3192G>A
ENST00000457511.6:c.742-3192G>A	ENSP00000401633.3:n.742-3192G>A
NM_001198950.1:c.742-3192G>A	NP_001185879.1:n.742-3192G>A
NM_015011.1:c.676-3192G>A	NP_055826.1:n.676-3192G>A
XM_011521062.1:c.676-3192G>A	XP_011519364.1:n.676-3192G>A
NM_001198950.2:c.742-3192G>A	NP_001185879.1:n.742-3192G>A
NM_015011.2:c.676-3192G>A	NP_055826.1:n.676-3192G>A
NM_001198950.3:c.742-3192G>A MANE Select	NP_001185879.1:n.742-3192G>A
NM_015011.3:c.676-3192G>A	NP_055826.1:n.676-3192G>A