Canonical Allele Identifier: CA2660687225
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947661_111947662insCTTCTTAAGGTCTATTCTCCAT , CM000664.2:g.111947661_111947662insCTTCTTAAGGTCTATTCTCCAT GRCh38
NC_000002.11:g.112705238_112705239insCTTCTTAAGGTCTATTCTCCAT , CM000664.1:g.112705238_112705239insCTTCTTAAGGTCTATTCTCCAT GRCh37
NC_000002.10:g.112421709_112421710insCTTCTTAAGGTCTATTCTCCAT NCBI36
NG_011607.1:g.54048_54049insCTTCTTAAGGTCTATTCTCCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT MANE Select ENSP00000295408.4:n.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT
ENST00000295408.8:c.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT ENSP00000295408.4:n.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT
ENST00000409780.5:c.229+94_229+95insCTTCTTAAGGTCTATTCTCCAT ENSP00000387277.1:n.229+94_229+95insCTTCTTAAGGTCTATTCTCCAT
ENST00000421804.6:c.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT ENSP00000389152.2:n.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT
ENST00000439966.5:c.*230+94_*230+95insCTTCTTAAGGTCTATTCTCCAT ENSP00000402129.1:n.*230+94_*230+95insCTTCTTAAGGTCTATTCTCCAT
ENST00000616902.4:c.-459+94_-459+95insCTTCTTAAGGTCTATTCTCCAT ENSP00000482824.1:n.-459+94_-459+95insCTTCTTAAGGTCTATTCTCCAT
NM_006343.2:c.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT NP_006334.2:n.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT
XM_005263565.3:c.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT XP_005263622.1:n.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT
XM_005263568.3:c.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT XP_005263625.1:n.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT
XM_011510490.1:c.568+94_568+95insCTTCTTAAGGTCTATTCTCCAT XP_011508792.1:n.568+94_568+95insCTTCTTAAGGTCTATTCTCCAT
XM_005263565.4:c.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT XP_005263622.1:n.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT
XM_005263568.4:c.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT XP_005263625.1:n.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT
XM_011510490.3:c.568+94_568+95insCTTCTTAAGGTCTATTCTCCAT XP_011508792.1:n.568+94_568+95insCTTCTTAAGGTCTATTCTCCAT
XM_017003164.1:c.568+94_568+95insCTTCTTAAGGTCTATTCTCCAT XP_016858653.1:n.568+94_568+95insCTTCTTAAGGTCTATTCTCCAT
XM_017003165.2:c.-511+94_-511+95insCTTCTTAAGGTCTATTCTCCAT XP_016858654.1:n.-511+94_-511+95insCTTCTTAAGGTCTATTCTCCAT
NM_006343.3:c.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT MANE Select NP_006334.2:n.757+94_757+95insCTTCTTAAGGTCTATTCTCCAT