Canonical Allele Identifier: CA1279544324
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947493A= , CM000664.2:g.111947493A= GRCh38
NC_000002.11:g.112705070A= , CM000664.1:g.112705070A= GRCh37
NC_000002.10:g.112421541A= NCBI36
NG_011607.1:g.53880A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.683A= MANE Select ENSP00000295408.4:p.Asn228=
ENST00000295408.8:c.683A= ENSP00000295408.4:p.Asn228=
ENST00000409780.5:c.155A= ENSP00000387277.1:p.Asn52=
ENST00000421804.6:c.683A= ENSP00000389152.2:p.Asn228=
ENST00000439966.5:c.*156A= ENSP00000402129.1:n.*156A=
ENST00000616902.4:c.-533A= ENSP00000482824.1:n.-533A=
NM_006343.2:c.683A= NP_006334.2:p.Asn228=
XM_005263565.3:c.683A= XP_005263622.1:p.Asn228=
XM_005263568.3:c.683A= XP_005263625.1:p.Asn228=
XM_011510490.1:c.494A= XP_011508792.1:p.Asn165=
XM_005263565.4:c.683A= XP_005263622.1:p.Asn228=
XM_005263568.4:c.683A= XP_005263625.1:p.Asn228=
XM_011510490.3:c.494A= XP_011508792.1:p.Asn165=
XM_017003164.1:c.494A= XP_016858653.1:p.Asn165=
XM_017003165.2:c.-585A= XP_016858654.1:n.-585A=
NM_006343.3:c.683A= MANE Select NP_006334.2:p.Asn228=