Canonical Allele Identifier: CA348230981
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111997335A>G , CM000664.2:g.111997335A>G GRCh38
NC_000002.11:g.112754912A>G , CM000664.1:g.112754912A>G GRCh37
NC_000002.10:g.112471383A>G NCBI36
NG_011607.1:g.103722A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.1463A>G MANE Select ENSP00000295408.4:p.Tyr488Cys
ENST00000295408.8:c.1463A>G ENSP00000295408.4:p.Tyr488Cys
ENST00000409780.5:c.935A>G ENSP00000387277.1:p.Tyr312Cys
ENST00000421804.6:c.1463A>G ENSP00000389152.2:p.Tyr488Cys
ENST00000439966.5:c.*936A>G ENSP00000402129.1:n.*936A>G
ENST00000616902.4:c.432A>G ENSP00000482824.1:p.Leu144=
NM_006343.2:c.1463A>G NP_006334.2:p.Tyr488Cys
XM_005263565.3:c.1463A>G XP_005263622.1:p.Tyr488Cys
XM_005263568.3:c.1463A>G XP_005263625.1:p.Tyr488Cys
XM_011510490.1:c.1274A>G XP_011508792.1:p.Tyr425Cys
XM_011510491.1:c.248A>G XP_011508793.1:p.Tyr83Cys
XM_005263565.4:c.1463A>G XP_005263622.1:p.Tyr488Cys
XM_005263568.4:c.1463A>G XP_005263625.1:p.Tyr488Cys
XM_011510490.3:c.1274A>G XP_011508792.1:p.Tyr425Cys
XM_017003164.1:c.1274A>G XP_016858653.1:p.Tyr425Cys
XM_017003165.2:c.248A>G XP_016858654.1:p.Tyr83Cys
NM_006343.3:c.1463A>G MANE Select NP_006334.2:p.Tyr488Cys