Canonical Allele Identifier: CA1279536520
Gene: MERTK HGNC NCBI

Linked Data

dbSNP Id: rs1684628392

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111929454_111929466del , CM000664.2:g.111929454_111929466del GRCh38
NC_000002.11:g.112687031_112687043del , CM000664.1:g.112687031_112687043del GRCh37
NC_000002.10:g.112403502_112403514del NCBI36
NG_011607.1:g.35841_35853del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.396_408del MANE Select ENSP00000295408.4:p.Lys132AsnfsTer21
ENST00000295408.8:c.396_408del ENSP00000295408.4:p.Lys132AsnfsTer21
ENST00000409780.5:c.-46-15506_-46-15494del ENSP00000387277.1:n.-46-15506_-46-15494del
ENST00000421804.6:c.396_408del ENSP00000389152.2:p.Lys132AsnfsTer21
ENST00000439966.5:c.246+150_246+162del ENSP00000402129.1:n.246+150_246+162del
ENST00000616902.4:c.-820_-808del ENSP00000482824.1:n.-820_-808del
NM_006343.2:c.396_408del NP_006334.2:p.Lys132AsnfsTer21
XM_005263565.3:c.396_408del XP_005263622.1:p.Lys132AsnfsTer21
XM_005263568.3:c.396_408del XP_005263625.1:p.Lys132AsnfsTer21
XM_011510490.1:c.207_219del XP_011508792.1:p.Lys69AsnfsTer21
XM_005263565.4:c.396_408del XP_005263622.1:p.Lys132AsnfsTer21
XM_005263568.4:c.396_408del XP_005263625.1:p.Lys132AsnfsTer21
XM_011510490.3:c.207_219del XP_011508792.1:p.Lys69AsnfsTer21
XM_017003164.1:c.207_219del XP_016858653.1:p.Lys69AsnfsTer21
XM_017003165.2:c.-872_-860del XP_016858654.1:n.-872_-860del
NM_006343.3:c.396_408del MANE Select NP_006334.2:p.Lys132AsnfsTer21