Canonical Allele Identifier: CA2660690151
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112008558_112008567del , CM000664.2:g.112008558_112008567del GRCh38
NC_000002.11:g.112766135_112766144del , CM000664.1:g.112766135_112766144del GRCh37
NC_000002.10:g.112482606_112482615del NCBI36
NG_011607.1:g.114945_114954del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.1960+83_1960+92del MANE Select ENSP00000295408.4:n.1960+83_1960+92del
ENST00000295408.8:c.1960+83_1960+92del ENSP00000295408.4:n.1960+83_1960+92del
ENST00000409780.5:c.1432+83_1432+92del ENSP00000387277.1:n.1432+83_1432+92del
ENST00000421804.6:c.1960+83_1960+92del ENSP00000389152.2:n.1960+83_1960+92del
ENST00000439966.5:c.*1433+83_*1433+92del ENSP00000402129.1:n.*1433+83_*1433+92del
ENST00000616902.4:c.925+83_925+92del ENSP00000482824.1:n.925+83_925+92del
NM_006343.2:c.1960+83_1960+92del NP_006334.2:n.1960+83_1960+92del
XM_005263565.3:c.1960+83_1960+92del XP_005263622.1:n.1960+83_1960+92del
XM_005263568.3:c.1960+83_1960+92del XP_005263625.1:n.1960+83_1960+92del
XM_011510490.1:c.1771+83_1771+92del XP_011508792.1:n.1771+83_1771+92del
XM_011510491.1:c.745+83_745+92del XP_011508793.1:n.745+83_745+92del
XM_005263565.4:c.1960+83_1960+92del XP_005263622.1:n.1960+83_1960+92del
XM_005263568.4:c.1960+83_1960+92del XP_005263625.1:n.1960+83_1960+92del
XM_011510490.3:c.1771+83_1771+92del XP_011508792.1:n.1771+83_1771+92del
XM_017003164.1:c.1771+83_1771+92del XP_016858653.1:n.1771+83_1771+92del
XM_017003165.2:c.745+83_745+92del XP_016858654.1:n.745+83_745+92del
NM_006343.3:c.1960+83_1960+92del MANE Select NP_006334.2:n.1960+83_1960+92del