Canonical Allele Identifier: CA1279544264

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947347_111947349delinsCTG , CM000664.2:g.111947347_111947349delinsCTG	GRCh38
NC_000002.11:g.112704924_112704926delinsCTG , CM000664.1:g.112704924_112704926delinsCTG	GRCh37
NC_000002.10:g.112421395_112421397delinsCTG	NCBI36
NG_011607.1:g.53734_53736delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.584-47_584-45delinsCTG MANE Select	ENSP00000295408.4:n.584-47_584-45delinsCTG
ENST00000295408.8:c.584-47_584-45delinsCTG	ENSP00000295408.4:n.584-47_584-45delinsCTG
ENST00000409780.5:c.56-47_56-45delinsCTG	ENSP00000387277.1:n.56-47_56-45delinsCTG
ENST00000421804.6:c.584-47_584-45delinsCTG	ENSP00000389152.2:n.584-47_584-45delinsCTG
ENST00000439966.5:c.*57-47_*57-45delinsCTG	ENSP00000402129.1:n.*57-47_*57-45delinsCTG
ENST00000616902.4:c.-632-47_-632-45delinsCTG	ENSP00000482824.1:n.-632-47_-632-45delinsCTG
NM_006343.2:c.584-47_584-45delinsCTG	NP_006334.2:n.584-47_584-45delinsCTG
XM_005263565.3:c.584-47_584-45delinsCTG	XP_005263622.1:n.584-47_584-45delinsCTG
XM_005263568.3:c.584-47_584-45delinsCTG	XP_005263625.1:n.584-47_584-45delinsCTG
XM_011510490.1:c.395-47_395-45delinsCTG	XP_011508792.1:n.395-47_395-45delinsCTG
XM_005263565.4:c.584-47_584-45delinsCTG	XP_005263622.1:n.584-47_584-45delinsCTG
XM_005263568.4:c.584-47_584-45delinsCTG	XP_005263625.1:n.584-47_584-45delinsCTG
XM_011510490.3:c.395-47_395-45delinsCTG	XP_011508792.1:n.395-47_395-45delinsCTG
XM_017003164.1:c.395-47_395-45delinsCTG	XP_016858653.1:n.395-47_395-45delinsCTG
XM_017003165.2:c.-684-47_-684-45delinsCTG	XP_016858654.1:n.-684-47_-684-45delinsCTG
NM_006343.3:c.584-47_584-45delinsCTG MANE Select	NP_006334.2:n.584-47_584-45delinsCTG