Canonical Allele Identifier: CA1035072743
Gene: MERTK HGNC NCBI

Linked Data

dbSNP Id: rs1677035843

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112008617_112008618insAAACAT , CM000664.2:g.112008617_112008618insAAACAT GRCh38
NC_000002.11:g.112766194_112766195insAAACAT , CM000664.1:g.112766194_112766195insAAACAT GRCh37
NC_000002.10:g.112482665_112482666insAAACAT NCBI36
NG_011607.1:g.115004_115005insAAACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.1960+142_1960+143insAAACAT MANE Select ENSP00000295408.4:n.1960+142_1960+143insAAACAT
ENST00000295408.8:c.1960+142_1960+143insAAACAT ENSP00000295408.4:n.1960+142_1960+143insAAACAT
ENST00000409780.5:c.1432+142_1432+143insAAACAT ENSP00000387277.1:n.1432+142_1432+143insAAACAT
ENST00000421804.6:c.1960+142_1960+143insAAACAT ENSP00000389152.2:n.1960+142_1960+143insAAACAT
ENST00000439966.5:c.*1433+142_*1433+143insAAACAT ENSP00000402129.1:n.*1433+142_*1433+143insAAACAT
ENST00000616902.4:c.925+142_925+143insAAACAT ENSP00000482824.1:n.925+142_925+143insAAACAT
NM_006343.2:c.1960+142_1960+143insAAACAT NP_006334.2:n.1960+142_1960+143insAAACAT
XM_005263565.3:c.1960+142_1960+143insAAACAT XP_005263622.1:n.1960+142_1960+143insAAACAT
XM_005263568.3:c.1960+142_1960+143insAAACAT XP_005263625.1:n.1960+142_1960+143insAAACAT
XM_011510490.1:c.1771+142_1771+143insAAACAT XP_011508792.1:n.1771+142_1771+143insAAACAT
XM_011510491.1:c.745+142_745+143insAAACAT XP_011508793.1:n.745+142_745+143insAAACAT
XM_005263565.4:c.1960+142_1960+143insAAACAT XP_005263622.1:n.1960+142_1960+143insAAACAT
XM_005263568.4:c.1960+142_1960+143insAAACAT XP_005263625.1:n.1960+142_1960+143insAAACAT
XM_011510490.3:c.1771+142_1771+143insAAACAT XP_011508792.1:n.1771+142_1771+143insAAACAT
XM_017003164.1:c.1771+142_1771+143insAAACAT XP_016858653.1:n.1771+142_1771+143insAAACAT
XM_017003165.2:c.745+142_745+143insAAACAT XP_016858654.1:n.745+142_745+143insAAACAT
NM_006343.3:c.1960+142_1960+143insAAACAT MANE Select NP_006334.2:n.1960+142_1960+143insAAACAT