Canonical Allele Identifier: CA1279544331
Gene: MERTK HGNC NCBI

Linked Data

dbSNP Id: rs1684981406

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947510_111947511del , CM000664.2:g.111947510_111947511del GRCh38
NC_000002.11:g.112705087_112705088del , CM000664.1:g.112705087_112705088del GRCh37
NC_000002.10:g.112421558_112421559del NCBI36
NG_011607.1:g.53897_53898del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.700_701del MANE Select ENSP00000295408.4:p.Asn234GlnfsTer2
ENST00000295408.8:c.700_701del ENSP00000295408.4:p.Asn234GlnfsTer2
ENST00000409780.5:c.172_173del ENSP00000387277.1:p.Asn58GlnfsTer2
ENST00000421804.6:c.700_701del ENSP00000389152.2:p.Asn234GlnfsTer2
ENST00000439966.5:c.*173_*174del ENSP00000402129.1:n.*173_*174del
ENST00000616902.4:c.-516_-515del ENSP00000482824.1:n.-516_-515del
NM_006343.2:c.700_701del NP_006334.2:p.Asn234GlnfsTer2
XM_005263565.3:c.700_701del XP_005263622.1:p.Asn234GlnfsTer2
XM_005263568.3:c.700_701del XP_005263625.1:p.Asn234GlnfsTer2
XM_011510490.1:c.511_512del XP_011508792.1:p.Asn171GlnfsTer2
XM_005263565.4:c.700_701del XP_005263622.1:p.Asn234GlnfsTer2
XM_005263568.4:c.700_701del XP_005263625.1:p.Asn234GlnfsTer2
XM_011510490.3:c.511_512del XP_011508792.1:p.Asn171GlnfsTer2
XM_017003164.1:c.511_512del XP_016858653.1:p.Asn171GlnfsTer2
XM_017003165.2:c.-568_-567del XP_016858654.1:n.-568_-567del
NM_006343.3:c.700_701del MANE Select NP_006334.2:p.Asn234GlnfsTer2