Canonical Allele Identifier: CA348229201
Gene: MERTK HGNC NCBI

Linked Data

dbSNP Id: rs1684981357

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947508A>G , CM000664.2:g.111947508A>G GRCh38
NC_000002.11:g.112705085A>G , CM000664.1:g.112705085A>G GRCh37
NC_000002.10:g.112421556A>G NCBI36
NG_011607.1:g.53895A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.698A>G MANE Select ENSP00000295408.4:p.Gln233Arg
ENST00000295408.8:c.698A>G ENSP00000295408.4:p.Gln233Arg
ENST00000409780.5:c.170A>G ENSP00000387277.1:p.Gln57Arg
ENST00000421804.6:c.698A>G ENSP00000389152.2:p.Gln233Arg
ENST00000439966.5:c.*171A>G ENSP00000402129.1:n.*171A>G
ENST00000616902.4:c.-518A>G ENSP00000482824.1:n.-518A>G
NM_006343.2:c.698A>G NP_006334.2:p.Gln233Arg
XM_005263565.3:c.698A>G XP_005263622.1:p.Gln233Arg
XM_005263568.3:c.698A>G XP_005263625.1:p.Gln233Arg
XM_011510490.1:c.509A>G XP_011508792.1:p.Gln170Arg
XM_005263565.4:c.698A>G XP_005263622.1:p.Gln233Arg
XM_005263568.4:c.698A>G XP_005263625.1:p.Gln233Arg
XM_011510490.3:c.509A>G XP_011508792.1:p.Gln170Arg
XM_017003164.1:c.509A>G XP_016858653.1:p.Gln170Arg
XM_017003165.2:c.-570A>G XP_016858654.1:n.-570A>G
NM_006343.3:c.698A>G MANE Select NP_006334.2:p.Gln233Arg