Canonical Allele Identifier: CA2751717265
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947551_111947552insACA , CM000664.2:g.111947551_111947552insACA GRCh38
NC_000002.11:g.112705128_112705129insACA , CM000664.1:g.112705128_112705129insACA GRCh37
NC_000002.10:g.112421599_112421600insACA NCBI36
NG_011607.1:g.53938_53939insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.741_742insACA MANE Select ENSP00000295408.4:p.Ser247_Val248insThr
ENST00000295408.8:c.741_742insACA ENSP00000295408.4:p.Ser247_Val248insThr
ENST00000409780.5:c.213_214insACA ENSP00000387277.1:p.Ser71_Val72insThr
ENST00000421804.6:c.741_742insACA ENSP00000389152.2:p.Ser247_Val248insThr
ENST00000439966.5:c.*214_*215insACA ENSP00000402129.1:n.*214_*215insACA
ENST00000616902.4:c.-475_-474insACA ENSP00000482824.1:n.-475_-474insACA
NM_006343.2:c.741_742insACA NP_006334.2:p.Ser247_Val248insThr
XM_005263565.3:c.741_742insACA XP_005263622.1:p.Ser247_Val248insThr
XM_005263568.3:c.741_742insACA XP_005263625.1:p.Ser247_Val248insThr
XM_011510490.1:c.552_553insACA XP_011508792.1:p.Ser184_Val185insThr
XM_005263565.4:c.741_742insACA XP_005263622.1:p.Ser247_Val248insThr
XM_005263568.4:c.741_742insACA XP_005263625.1:p.Ser247_Val248insThr
XM_011510490.3:c.552_553insACA XP_011508792.1:p.Ser184_Val185insThr
XM_017003164.1:c.552_553insACA XP_016858653.1:p.Ser184_Val185insThr
XM_017003165.2:c.-527_-526insACA XP_016858654.1:n.-527_-526insACA
NM_006343.3:c.741_742insACA MANE Select NP_006334.2:p.Ser247_Val248insThr