Canonical Allele Identifier: CA1279544347
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947543_111947544delinsTC , CM000664.2:g.111947543_111947544delinsTC GRCh38
NC_000002.11:g.112705120_112705121delinsTC , CM000664.1:g.112705120_112705121delinsTC GRCh37
NC_000002.10:g.112421591_112421592delinsTC NCBI36
NG_011607.1:g.53930_53931delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.733_734delinsTC MANE Select ENSP00000295408.4:p.Ser245=
ENST00000295408.8:c.733_734delinsTC ENSP00000295408.4:p.Ser245=
ENST00000409780.5:c.205_206delinsTC ENSP00000387277.1:p.Ser69=
ENST00000421804.6:c.733_734delinsTC ENSP00000389152.2:p.Ser245=
ENST00000439966.5:c.*206_*207delinsTC ENSP00000402129.1:n.*206_*207delinsTC
ENST00000616902.4:c.-483_-482delinsTC ENSP00000482824.1:n.-483_-482delinsTC
NM_006343.2:c.733_734delinsTC NP_006334.2:p.Ser245=
XM_005263565.3:c.733_734delinsTC XP_005263622.1:p.Ser245=
XM_005263568.3:c.733_734delinsTC XP_005263625.1:p.Ser245=
XM_011510490.1:c.544_545delinsTC XP_011508792.1:p.Ser182=
XM_005263565.4:c.733_734delinsTC XP_005263622.1:p.Ser245=
XM_005263568.4:c.733_734delinsTC XP_005263625.1:p.Ser245=
XM_011510490.3:c.544_545delinsTC XP_011508792.1:p.Ser182=
XM_017003164.1:c.544_545delinsTC XP_016858653.1:p.Ser182=
XM_017003165.2:c.-535_-534delinsTC XP_016858654.1:n.-535_-534delinsTC
NM_006343.3:c.733_734delinsTC MANE Select NP_006334.2:p.Ser245=