Canonical Allele Identifier: CA2660687123
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947306_111947307insCA , CM000664.2:g.111947306_111947307insCA GRCh38
NC_000002.11:g.112704883_112704884insCA , CM000664.1:g.112704883_112704884insCA GRCh37
NC_000002.10:g.112421354_112421355insCA NCBI36
NG_011607.1:g.53693_53694insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.584-88_584-87insCA MANE Select ENSP00000295408.4:n.584-88_584-87insCA
ENST00000295408.8:c.584-88_584-87insCA ENSP00000295408.4:n.584-88_584-87insCA
ENST00000409780.5:c.56-88_56-87insCA ENSP00000387277.1:n.56-88_56-87insCA
ENST00000421804.6:c.584-88_584-87insCA ENSP00000389152.2:n.584-88_584-87insCA
ENST00000439966.5:c.*57-88_*57-87insCA ENSP00000402129.1:n.*57-88_*57-87insCA
ENST00000616902.4:c.-632-88_-632-87insCA ENSP00000482824.1:n.-632-88_-632-87insCA
NM_006343.2:c.584-88_584-87insCA NP_006334.2:n.584-88_584-87insCA
XM_005263565.3:c.584-88_584-87insCA XP_005263622.1:n.584-88_584-87insCA
XM_005263568.3:c.584-88_584-87insCA XP_005263625.1:n.584-88_584-87insCA
XM_011510490.1:c.395-88_395-87insCA XP_011508792.1:n.395-88_395-87insCA
XM_005263565.4:c.584-88_584-87insCA XP_005263622.1:n.584-88_584-87insCA
XM_005263568.4:c.584-88_584-87insCA XP_005263625.1:n.584-88_584-87insCA
XM_011510490.3:c.395-88_395-87insCA XP_011508792.1:n.395-88_395-87insCA
XM_017003164.1:c.395-88_395-87insCA XP_016858653.1:n.395-88_395-87insCA
XM_017003165.2:c.-684-88_-684-87insCA XP_016858654.1:n.-684-88_-684-87insCA
NM_006343.3:c.584-88_584-87insCA MANE Select NP_006334.2:n.584-88_584-87insCA