Canonical Allele Identifier: CA2660687168
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947372_111947373dup , CM000664.2:g.111947372_111947373dup GRCh38
NC_000002.11:g.112704949_112704950dup , CM000664.1:g.112704949_112704950dup GRCh37
NC_000002.10:g.112421420_112421421dup NCBI36
NG_011607.1:g.53759_53760dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.584-22_584-21dup MANE Select ENSP00000295408.4:n.584-22_584-21dup
ENST00000295408.8:c.584-22_584-21dup ENSP00000295408.4:n.584-22_584-21dup
ENST00000409780.5:c.56-22_56-21dup ENSP00000387277.1:n.56-22_56-21dup
ENST00000421804.6:c.584-22_584-21dup ENSP00000389152.2:n.584-22_584-21dup
ENST00000439966.5:c.*57-22_*57-21dup ENSP00000402129.1:n.*57-22_*57-21dup
ENST00000616902.4:c.-632-22_-632-21dup ENSP00000482824.1:n.-632-22_-632-21dup
NM_006343.2:c.584-22_584-21dup NP_006334.2:n.584-22_584-21dup
XM_005263565.3:c.584-22_584-21dup XP_005263622.1:n.584-22_584-21dup
XM_005263568.3:c.584-22_584-21dup XP_005263625.1:n.584-22_584-21dup
XM_011510490.1:c.395-22_395-21dup XP_011508792.1:n.395-22_395-21dup
XM_005263565.4:c.584-22_584-21dup XP_005263622.1:n.584-22_584-21dup
XM_005263568.4:c.584-22_584-21dup XP_005263625.1:n.584-22_584-21dup
XM_011510490.3:c.395-22_395-21dup XP_011508792.1:n.395-22_395-21dup
XM_017003164.1:c.395-22_395-21dup XP_016858653.1:n.395-22_395-21dup
XM_017003165.2:c.-684-22_-684-21dup XP_016858654.1:n.-684-22_-684-21dup
NM_006343.3:c.584-22_584-21dup MANE Select NP_006334.2:n.584-22_584-21dup