Canonical Allele Identifier: CA348239093
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.112021494C>A , CM000664.2:g.112021494C>A GRCh38
NC_000002.11:g.112779071C>A , CM000664.1:g.112779071C>A GRCh37
NC_000002.10:g.112495542C>A NCBI36
NG_011607.1:g.127881C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.2262C>A MANE Select ENSP00000295408.4:p.Tyr754Ter
ENST00000295408.8:c.2262C>A ENSP00000295408.4:p.Tyr754Ter
ENST00000409780.5:c.1734C>A ENSP00000387277.1:p.Tyr578Ter
ENST00000421804.6:c.2262C>A ENSP00000389152.2:p.Tyr754Ter
ENST00000439966.5:c.*1735C>A ENSP00000402129.1:n.*1735C>A
ENST00000449344.2:c.234C>A ENSP00000412660.2:p.Tyr78Ter
ENST00000616902.4:c.1218C>A ENSP00000482824.1:p.Tyr406Ter
NM_006343.2:c.2262C>A NP_006334.2:p.Tyr754Ter
XM_005263565.3:c.2262C>A XP_005263622.1:p.Tyr754Ter
XM_011510490.1:c.2073C>A XP_011508792.1:p.Tyr691Ter
XM_011510491.1:c.1047C>A XP_011508793.1:p.Tyr349Ter
XM_005263565.4:c.2262C>A XP_005263622.1:p.Tyr754Ter
XM_011510490.3:c.2073C>A XP_011508792.1:p.Tyr691Ter
XM_017003164.1:c.2073C>A XP_016858653.1:p.Tyr691Ter
XM_017003165.2:c.1047C>A XP_016858654.1:p.Tyr349Ter
NM_006343.3:c.2262C>A MANE Select NP_006334.2:p.Tyr754Ter