Canonical Allele Identifier: CA2751717258
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947520_111947529del , CM000664.2:g.111947520_111947529del GRCh38
NC_000002.11:g.112705097_112705106del , CM000664.1:g.112705097_112705106del GRCh37
NC_000002.10:g.112421568_112421577del NCBI36
NG_011607.1:g.53907_53916del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.710_719del MANE Select ENSP00000295408.4:p.Arg237HisfsTer10
ENST00000295408.8:c.710_719del ENSP00000295408.4:p.Arg237HisfsTer10
ENST00000409780.5:c.182_191del ENSP00000387277.1:p.Arg61HisfsTer10
ENST00000421804.6:c.710_719del ENSP00000389152.2:p.Arg237HisfsTer10
ENST00000439966.5:c.*183_*192del ENSP00000402129.1:n.*183_*192del
ENST00000616902.4:c.-506_-497del ENSP00000482824.1:n.-506_-497del
NM_006343.2:c.710_719del NP_006334.2:p.Arg237HisfsTer10
XM_005263565.3:c.710_719del XP_005263622.1:p.Arg237HisfsTer10
XM_005263568.3:c.710_719del XP_005263625.1:p.Arg237HisfsTer10
XM_011510490.1:c.521_530del XP_011508792.1:p.Arg174HisfsTer10
XM_005263565.4:c.710_719del XP_005263622.1:p.Arg237HisfsTer10
XM_005263568.4:c.710_719del XP_005263625.1:p.Arg237HisfsTer10
XM_011510490.3:c.521_530del XP_011508792.1:p.Arg174HisfsTer10
XM_017003164.1:c.521_530del XP_016858653.1:p.Arg174HisfsTer10
XM_017003165.2:c.-558_-549del XP_016858654.1:n.-558_-549del
NM_006343.3:c.710_719del MANE Select NP_006334.2:p.Arg237HisfsTer10