Canonical Allele Identifier: CA1279566609
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111997500T= , CM000664.2:g.111997500T= GRCh38
NC_000002.11:g.112755077T= , CM000664.1:g.112755077T= GRCh37
NC_000002.10:g.112471548T= NCBI36
NG_011607.1:g.103887T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295408.9:c.1604+24T= MANE Select ENSP00000295408.4:n.1604+24T=
ENST00000295408.8:c.1604+24T= ENSP00000295408.4:n.1604+24T=
ENST00000409780.5:c.1076+24T= ENSP00000387277.1:n.1076+24T=
ENST00000421804.6:c.1604+24T= ENSP00000389152.2:n.1604+24T=
ENST00000439966.5:c.*1077+24T= ENSP00000402129.1:n.*1077+24T=
ENST00000473065.1:n.107+24T=
ENST00000616902.4:c.569+24T= ENSP00000482824.1:n.569+24T=
NM_006343.2:c.1604+24T= NP_006334.2:n.1604+24T=
XM_005263565.3:c.1604+24T= XP_005263622.1:n.1604+24T=
XM_005263568.3:c.1604+24T= XP_005263625.1:n.1604+24T=
XM_011510490.1:c.1415+24T= XP_011508792.1:n.1415+24T=
XM_011510491.1:c.389+24T= XP_011508793.1:n.389+24T=
XM_005263565.4:c.1604+24T= XP_005263622.1:n.1604+24T=
XM_005263568.4:c.1604+24T= XP_005263625.1:n.1604+24T=
XM_011510490.3:c.1415+24T= XP_011508792.1:n.1415+24T=
XM_017003164.1:c.1415+24T= XP_016858653.1:n.1415+24T=
XM_017003165.2:c.389+24T= XP_016858654.1:n.389+24T=
NM_006343.3:c.1604+24T= MANE Select NP_006334.2:n.1604+24T=