Canonical Allele Identifier: CA2586969798
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947565del , CM000664.2:g.111947565del GRCh38
NC_000002.11:g.112705142del , CM000664.1:g.112705142del GRCh37
NC_000002.10:g.112421613del NCBI36
NG_011607.1:g.53952del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.755del MANE Select ENSP00000295408.4:p.Pro252GlnfsTer3
ENST00000295408.8:c.755del ENSP00000295408.4:p.Pro252GlnfsTer3
ENST00000409780.5:c.227del ENSP00000387277.1:p.Pro76GlnfsTer3
ENST00000421804.6:c.755del ENSP00000389152.2:p.Pro252GlnfsTer3
ENST00000439966.5:c.*228del ENSP00000402129.1:n.*228del
ENST00000616902.4:c.-461del ENSP00000482824.1:n.-461del
NM_006343.2:c.755del NP_006334.2:p.Pro252GlnfsTer3
XM_005263565.3:c.755del XP_005263622.1:p.Pro252GlnfsTer3
XM_005263568.3:c.755del XP_005263625.1:p.Pro252GlnfsTer3
XM_011510490.1:c.566del XP_011508792.1:p.Pro189GlnfsTer3
XM_005263565.4:c.755del XP_005263622.1:p.Pro252GlnfsTer3
XM_005263568.4:c.755del XP_005263625.1:p.Pro252GlnfsTer3
XM_011510490.3:c.566del XP_011508792.1:p.Pro189GlnfsTer3
XM_017003164.1:c.566del XP_016858653.1:p.Pro189GlnfsTer3
XM_017003165.2:c.-513del XP_016858654.1:n.-513del
NM_006343.3:c.755del MANE Select NP_006334.2:p.Pro252GlnfsTer3