Canonical Allele Identifier: CA2751717236
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947301_111947302insAATT , CM000664.2:g.111947301_111947302insAATT GRCh38
NC_000002.11:g.112704878_112704879insAATT , CM000664.1:g.112704878_112704879insAATT GRCh37
NC_000002.10:g.112421349_112421350insAATT NCBI36
NG_011607.1:g.53688_53689insAATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.584-93_584-92insAATT MANE Select ENSP00000295408.4:n.584-93_584-92insAATT
ENST00000295408.8:c.584-93_584-92insAATT ENSP00000295408.4:n.584-93_584-92insAATT
ENST00000409780.5:c.56-93_56-92insAATT ENSP00000387277.1:n.56-93_56-92insAATT
ENST00000421804.6:c.584-93_584-92insAATT ENSP00000389152.2:n.584-93_584-92insAATT
ENST00000439966.5:c.*57-93_*57-92insAATT ENSP00000402129.1:n.*57-93_*57-92insAATT
ENST00000616902.4:c.-632-93_-632-92insAATT ENSP00000482824.1:n.-632-93_-632-92insAATT
NM_006343.2:c.584-93_584-92insAATT NP_006334.2:n.584-93_584-92insAATT
XM_005263565.3:c.584-93_584-92insAATT XP_005263622.1:n.584-93_584-92insAATT
XM_005263568.3:c.584-93_584-92insAATT XP_005263625.1:n.584-93_584-92insAATT
XM_011510490.1:c.395-93_395-92insAATT XP_011508792.1:n.395-93_395-92insAATT
XM_005263565.4:c.584-93_584-92insAATT XP_005263622.1:n.584-93_584-92insAATT
XM_005263568.4:c.584-93_584-92insAATT XP_005263625.1:n.584-93_584-92insAATT
XM_011510490.3:c.395-93_395-92insAATT XP_011508792.1:n.395-93_395-92insAATT
XM_017003164.1:c.395-93_395-92insAATT XP_016858653.1:n.395-93_395-92insAATT
XM_017003165.2:c.-684-93_-684-92insAATT XP_016858654.1:n.-684-93_-684-92insAATT
NM_006343.3:c.584-93_584-92insAATT MANE Select NP_006334.2:n.584-93_584-92insAATT