Canonical Allele Identifier: CA2660687069

Gene: MERTK

Linked Data

• gnomAD v4: 2-111947297-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947297_111947298insC , CM000664.2:g.111947297_111947298insC	GRCh38
NC_000002.11:g.112704874_112704875insC , CM000664.1:g.112704874_112704875insC	GRCh37
NC_000002.10:g.112421345_112421346insC	NCBI36
NG_011607.1:g.53684_53685insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.584-97_584-96insC MANE Select	ENSP00000295408.4:n.584-97_584-96insC
ENST00000295408.8:c.584-97_584-96insC	ENSP00000295408.4:n.584-97_584-96insC
ENST00000409780.5:c.56-97_56-96insC	ENSP00000387277.1:n.56-97_56-96insC
ENST00000421804.6:c.584-97_584-96insC	ENSP00000389152.2:n.584-97_584-96insC
ENST00000439966.5:c.*57-97_*57-96insC	ENSP00000402129.1:n.*57-97_*57-96insC
ENST00000616902.4:c.-632-97_-632-96insC	ENSP00000482824.1:n.-632-97_-632-96insC
NM_006343.2:c.584-97_584-96insC	NP_006334.2:n.584-97_584-96insC
XM_005263565.3:c.584-97_584-96insC	XP_005263622.1:n.584-97_584-96insC
XM_005263568.3:c.584-97_584-96insC	XP_005263625.1:n.584-97_584-96insC
XM_011510490.1:c.395-97_395-96insC	XP_011508792.1:n.395-97_395-96insC
XM_005263565.4:c.584-97_584-96insC	XP_005263622.1:n.584-97_584-96insC
XM_005263568.4:c.584-97_584-96insC	XP_005263625.1:n.584-97_584-96insC
XM_011510490.3:c.395-97_395-96insC	XP_011508792.1:n.395-97_395-96insC
XM_017003164.1:c.395-97_395-96insC	XP_016858653.1:n.395-97_395-96insC
XM_017003165.2:c.-684-97_-684-96insC	XP_016858654.1:n.-684-97_-684-96insC
NM_006343.3:c.584-97_584-96insC MANE Select	NP_006334.2:n.584-97_584-96insC