Canonical Allele Identifier: CA2586545547
Gene: MYH14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50268345_50268347del , CM000681.2:g.50268345_50268347del GRCh38
NC_000019.9:g.50771602_50771604del , CM000681.1:g.50771602_50771604del GRCh37
NC_000019.8:g.55463414_55463416del NCBI36
NG_011645.1:g.69718_69720del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425460.6:c.2912_2914del ENSP00000407879.1:p.Lys971del
ENST00000642316.2:c.3011_3013del MANE Select ENSP00000493594.1:p.Lys1004del
ENST00000376970.6:c.2888_2890del ENSP00000366169.3:p.Lys963del
ENST00000425460.5:c.2912_2914del ENSP00000407879.1:p.Lys971del
ENST00000440075.6:c.-727-7646_-727-7644del ENSP00000406273.3:n.-727-7646_-727-7644del
ENST00000596571.5:c.2888_2890del ENSP00000472819.1:p.Lys963del
ENST00000598205.5:c.2912_2914del ENSP00000472543.1:p.Lys971del
ENST00000599920.5:c.2912_2914del ENSP00000469573.1:p.Lys971del
ENST00000601313.5:c.3011_3013del ENSP00000470298.1:p.Lys1004del
NM_001077186.1:c.2912_2914del NP_001070654.1:p.Lys971del
NM_001145809.1:c.3011_3013del NP_001139281.1:p.Lys1004del
NM_024729.3:c.2888_2890del NP_079005.3:p.Lys963del
XM_006723386.2:c.2912_2914del XP_006723449.1:p.Lys971del
XM_011527320.1:c.3032_3034del XP_011525622.1:p.Lys1011del
XM_011527321.1:c.3008_3010del XP_011525623.1:p.Lys1003del
XM_011527322.1:c.2936_2938del XP_011525624.1:p.Lys979del
XM_011527323.1:c.2912_2914del XP_011525625.1:p.Lys971del
XM_006723386.4:c.2912_2914del XP_006723449.1:p.Lys971del
XM_011527320.2:c.3032_3034del XP_011525622.1:p.Lys1011del
XM_011527321.2:c.3008_3010del XP_011525623.1:p.Lys1003del
XM_011527323.2:c.2912_2914del XP_011525625.1:p.Lys971del
XM_024451721.1:c.2888_2890del XP_024307489.1:p.Lys963del
NM_001077186.2:c.2912_2914del NP_001070654.1:p.Lys971del
NM_001145809.2:c.3011_3013del MANE Select NP_001139281.1:p.Lys1004del
NM_024729.4:c.2888_2890del NP_079005.3:p.Lys963del