Canonical Allele Identifier: CA2751717261
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947542dup , CM000664.2:g.111947542dup GRCh38
NC_000002.11:g.112705119dup , CM000664.1:g.112705119dup GRCh37
NC_000002.10:g.112421590dup NCBI36
NG_011607.1:g.53929dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.732dup MANE Select ENSP00000295408.4:p.Ser245IlefsTer19
ENST00000295408.8:c.732dup ENSP00000295408.4:p.Ser245IlefsTer19
ENST00000409780.5:c.204dup ENSP00000387277.1:p.Ser69IlefsTer19
ENST00000421804.6:c.732dup ENSP00000389152.2:p.Ser245IlefsTer19
ENST00000439966.5:c.*205dup ENSP00000402129.1:n.*205dup
ENST00000616902.4:c.-484dup ENSP00000482824.1:n.-484dup
NM_006343.2:c.732dup NP_006334.2:p.Ser245IlefsTer19
XM_005263565.3:c.732dup XP_005263622.1:p.Ser245IlefsTer19
XM_005263568.3:c.732dup XP_005263625.1:p.Ser245IlefsTer19
XM_011510490.1:c.543dup XP_011508792.1:p.Ser182IlefsTer19
XM_005263565.4:c.732dup XP_005263622.1:p.Ser245IlefsTer19
XM_005263568.4:c.732dup XP_005263625.1:p.Ser245IlefsTer19
XM_011510490.3:c.543dup XP_011508792.1:p.Ser182IlefsTer19
XM_017003164.1:c.543dup XP_016858653.1:p.Ser182IlefsTer19
XM_017003165.2:c.-536dup XP_016858654.1:n.-536dup
NM_006343.3:c.732dup MANE Select NP_006334.2:p.Ser245IlefsTer19