Canonical Allele Identifier: CA9158855

Gene: MYO1F

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8526894G>T , CM000681.2:g.8526894G>T	GRCh38
NC_000019.9:g.8591778G>T , CM000681.1:g.8591778G>T	GRCh37
NC_000019.8:g.8497778G>T	NCBI36
NG_052844.1:g.55554C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012335.4:c.2516C>A MANE Select	NP_036467.2:p.Ala839Asp
ENST00000644032.2:c.2516C>A MANE Select	ENSP00000494550.1:p.Ala839Asp
NM_001348355.1:c.2504C>A	NP_001335284.1:p.Ala835Asp
NM_001348355.2:c.2504C>A	NP_001335284.1:p.Ala835Asp
NM_012335.3:c.2516C>A	NP_036467.2:p.Ala839Asp
ENST00000338257.12:c.2516C>A	ENSP00000344871.6:p.Ala839Asp
ENST00000598005.1:c.999C>A	ENSP00000469098.1:n.999C>A
ENST00000600885.1:n.92C>A
ENST00000613525.4:c.2516C>A	ENSP00000481682.1:p.Ala839Asp
XM_011528024.1:c.2579C>A	XP_011526326.1:p.Ala860Asp
XM_011528024.2:c.2579C>A	XP_011526326.1:p.Ala860Asp
XM_011528025.1:c.2567C>A	XP_011526327.1:p.Ala856Asp
XM_011528025.2:c.2567C>A	XP_011526327.1:p.Ala856Asp
XM_011528026.1:c.2492C>A	XP_011526328.1:p.Ala831Asp
XM_011528026.2:c.2492C>A	XP_011526328.1:p.Ala831Asp
XM_011528027.1:c.2444C>A	XP_011526329.1:p.Ala815Asp
XM_011528027.2:c.2444C>A	XP_011526329.1:p.Ala815Asp
XM_024451522.1:c.1361C>A	XP_024307290.1:p.Ala454Asp
XR_001753692.2:n.2698C>A
XR_936179.1:n.2703C>A