Canonical Allele Identifier: CA2751719124
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111997441_111997442insT , CM000664.2:g.111997441_111997442insT GRCh38
NC_000002.11:g.112755018_112755019insT , CM000664.1:g.112755018_112755019insT GRCh37
NC_000002.10:g.112471489_112471490insT NCBI36
NG_011607.1:g.103828_103829insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.1569_1570insT MANE Select ENSP00000295408.4:p.Ala524CysfsTer21
ENST00000295408.8:c.1569_1570insT ENSP00000295408.4:p.Ala524CysfsTer21
ENST00000409780.5:c.1041_1042insT ENSP00000387277.1:p.Ala348CysfsTer21
ENST00000421804.6:c.1569_1570insT ENSP00000389152.2:p.Ala524CysfsTer21
ENST00000439966.5:c.*1042_*1043insT ENSP00000402129.1:n.*1042_*1043insT
ENST00000473065.1:n.72_73insT
ENST00000616902.4:c.534_535insT ENSP00000482824.1:p.Ala179CysfsTer21
NM_006343.2:c.1569_1570insT NP_006334.2:p.Ala524CysfsTer21
XM_005263565.3:c.1569_1570insT XP_005263622.1:p.Ala524CysfsTer21
XM_005263568.3:c.1569_1570insT XP_005263625.1:p.Ala524CysfsTer21
XM_011510490.1:c.1380_1381insT XP_011508792.1:p.Ala461CysfsTer21
XM_011510491.1:c.354_355insT XP_011508793.1:p.Ala119CysfsTer21
XM_005263565.4:c.1569_1570insT XP_005263622.1:p.Ala524CysfsTer21
XM_005263568.4:c.1569_1570insT XP_005263625.1:p.Ala524CysfsTer21
XM_011510490.3:c.1380_1381insT XP_011508792.1:p.Ala461CysfsTer21
XM_017003164.1:c.1380_1381insT XP_016858653.1:p.Ala461CysfsTer21
XM_017003165.2:c.354_355insT XP_016858654.1:p.Ala119CysfsTer21
NM_006343.3:c.1569_1570insT MANE Select NP_006334.2:p.Ala524CysfsTer21