Canonical Allele Identifier: CA252137
Gene: MYH14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2200
dbSNP Id: rs119103281

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50210724C>T , CM000681.2:g.50210724C>T GRCh38
NC_000019.9:g.50713981C>T , CM000681.1:g.50713981C>T GRCh37
NC_000019.8:g.55405793C>T NCBI36
NG_011645.1:g.12097C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000425460.6:c.359C>T ENSP00000407879.1:p.Ser120Leu
ENST00000642316.2:c.359C>T MANE Select ENSP00000493594.1:p.Ser120Leu
ENST00000642980.1:c.359C>T ENSP00000493650.1:p.Ser120Leu
ENST00000646861.1:c.359C>T ENSP00000493667.1:p.Ser120Leu
ENST00000376970.6:c.359C>T ENSP00000366169.3:p.Ser120Leu
ENST00000425460.5:c.359C>T ENSP00000407879.1:p.Ser120Leu
ENST00000440075.6:c.-1932C>T ENSP00000406273.3:n.-1932C>T
ENST00000596571.5:c.359C>T ENSP00000472819.1:p.Ser120Leu
ENST00000598205.5:c.359C>T ENSP00000472543.1:p.Ser120Leu
ENST00000599920.5:c.359C>T ENSP00000469573.1:p.Ser120Leu
ENST00000601313.5:c.359C>T ENSP00000470298.1:p.Ser120Leu
NM_001077186.1:c.359C>T NP_001070654.1:p.Ser120Leu
NM_001145809.1:c.359C>T NP_001139281.1:p.Ser120Leu
NM_024729.3:c.359C>T NP_079005.3:p.Ser120Leu
XM_006723386.2:c.359C>T XP_006723449.1:p.Ser120Leu
XM_011527320.1:c.479C>T XP_011525622.1:p.Ser160Leu
XM_011527321.1:c.479C>T XP_011525623.1:p.Ser160Leu
XM_011527322.1:c.479C>T XP_011525624.1:p.Ser160Leu
XM_011527323.1:c.359C>T XP_011525625.1:p.Ser120Leu
XM_006723386.4:c.359C>T XP_006723449.1:p.Ser120Leu
XM_011527320.2:c.479C>T XP_011525622.1:p.Ser160Leu
XM_011527321.2:c.479C>T XP_011525623.1:p.Ser160Leu
XM_011527323.2:c.359C>T XP_011525625.1:p.Ser120Leu
XM_024451721.1:c.359C>T XP_024307489.1:p.Ser120Leu
NM_001077186.2:c.359C>T NP_001070654.1:p.Ser120Leu
NM_001145809.2:c.359C>T MANE Select NP_001139281.1:p.Ser120Leu
NM_024729.4:c.359C>T NP_079005.3:p.Ser120Leu