Canonical Allele Identifier: CA2751719115
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111997398_111997399insAC , CM000664.2:g.111997398_111997399insAC GRCh38
NC_000002.11:g.112754975_112754976insAC , CM000664.1:g.112754975_112754976insAC GRCh37
NC_000002.10:g.112471446_112471447insAC NCBI36
NG_011607.1:g.103785_103786insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.1526_1527insAC MANE Select ENSP00000295408.4:p.Phe509LeufsTer7
ENST00000295408.8:c.1526_1527insAC ENSP00000295408.4:p.Phe509LeufsTer7
ENST00000409780.5:c.998_999insAC ENSP00000387277.1:p.Phe333LeufsTer7
ENST00000421804.6:c.1526_1527insAC ENSP00000389152.2:p.Phe509LeufsTer7
ENST00000439966.5:c.*999_*1000insAC ENSP00000402129.1:n.*999_*1000insAC
ENST00000473065.1:n.29_30insAC
ENST00000616902.4:c.495_496insAC ENSP00000482824.1:p.Leu166ThrfsTer5
NM_006343.2:c.1526_1527insAC NP_006334.2:p.Phe509LeufsTer7
XM_005263565.3:c.1526_1527insAC XP_005263622.1:p.Phe509LeufsTer7
XM_005263568.3:c.1526_1527insAC XP_005263625.1:p.Phe509LeufsTer7
XM_011510490.1:c.1337_1338insAC XP_011508792.1:p.Phe446LeufsTer7
XM_011510491.1:c.311_312insAC XP_011508793.1:p.Phe104LeufsTer7
XM_005263565.4:c.1526_1527insAC XP_005263622.1:p.Phe509LeufsTer7
XM_005263568.4:c.1526_1527insAC XP_005263625.1:p.Phe509LeufsTer7
XM_011510490.3:c.1337_1338insAC XP_011508792.1:p.Phe446LeufsTer7
XM_017003164.1:c.1337_1338insAC XP_016858653.1:p.Phe446LeufsTer7
XM_017003165.2:c.311_312insAC XP_016858654.1:p.Phe104LeufsTer7
NM_006343.3:c.1526_1527insAC MANE Select NP_006334.2:p.Phe509LeufsTer7