Canonical Allele Identifier: CA2586545548
Gene: MYH14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50268342del , CM000681.2:g.50268342del GRCh38
NC_000019.9:g.50771599del , CM000681.1:g.50771599del GRCh37
NC_000019.8:g.55463411del NCBI36
NG_011645.1:g.69715del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425460.6:c.2909del ENSP00000407879.1:p.Lys970ArgfsTer11
ENST00000642316.2:c.3008del MANE Select ENSP00000493594.1:p.Lys1003ArgfsTer11
ENST00000376970.6:c.2885del ENSP00000366169.3:p.Lys962ArgfsTer11
ENST00000425460.5:c.2909del ENSP00000407879.1:p.Lys970ArgfsTer11
ENST00000440075.6:c.-727-7649del ENSP00000406273.3:n.-727-7649del
ENST00000596571.5:c.2885del ENSP00000472819.1:p.Lys962ArgfsTer11
ENST00000598205.5:c.2909del ENSP00000472543.1:p.Lys970ArgfsTer11
ENST00000599920.5:c.2909del ENSP00000469573.1:p.Lys970ArgfsTer11
ENST00000601313.5:c.3008del ENSP00000470298.1:p.Lys1003ArgfsTer11
NM_001077186.1:c.2909del NP_001070654.1:p.Lys970ArgfsTer11
NM_001145809.1:c.3008del NP_001139281.1:p.Lys1003ArgfsTer11
NM_024729.3:c.2885del NP_079005.3:p.Lys962ArgfsTer11
XM_006723386.2:c.2909del XP_006723449.1:p.Lys970ArgfsTer11
XM_011527320.1:c.3029del XP_011525622.1:p.Lys1010ArgfsTer11
XM_011527321.1:c.3005del XP_011525623.1:p.Lys1002ArgfsTer11
XM_011527322.1:c.2933del XP_011525624.1:p.Lys978ArgfsTer11
XM_011527323.1:c.2909del XP_011525625.1:p.Lys970ArgfsTer11
XM_006723386.4:c.2909del XP_006723449.1:p.Lys970ArgfsTer11
XM_011527320.2:c.3029del XP_011525622.1:p.Lys1010ArgfsTer11
XM_011527321.2:c.3005del XP_011525623.1:p.Lys1002ArgfsTer11
XM_011527323.2:c.2909del XP_011525625.1:p.Lys970ArgfsTer11
XM_024451721.1:c.2885del XP_024307489.1:p.Lys962ArgfsTer11
NM_001077186.2:c.2909del NP_001070654.1:p.Lys970ArgfsTer11
NM_001145809.2:c.3008del MANE Select NP_001139281.1:p.Lys1003ArgfsTer11
NM_024729.4:c.2885del NP_079005.3:p.Lys962ArgfsTer11