Canonical Allele Identifier: CA2660687048

Gene: MERTK

Linked Data

• gnomAD v4: 2-111947295-AAAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947296_111947298del , CM000664.2:g.111947296_111947298del	GRCh38
NC_000002.11:g.112704873_112704875del , CM000664.1:g.112704873_112704875del	GRCh37
NC_000002.10:g.112421344_112421346del	NCBI36
NG_011607.1:g.53683_53685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.584-98_584-96del MANE Select	ENSP00000295408.4:n.584-98_584-96del
ENST00000295408.8:c.584-98_584-96del	ENSP00000295408.4:n.584-98_584-96del
ENST00000409780.5:c.56-98_56-96del	ENSP00000387277.1:n.56-98_56-96del
ENST00000421804.6:c.584-98_584-96del	ENSP00000389152.2:n.584-98_584-96del
ENST00000439966.5:c.*57-98_*57-96del	ENSP00000402129.1:n.*57-98_*57-96del
ENST00000616902.4:c.-632-98_-632-96del	ENSP00000482824.1:n.-632-98_-632-96del
NM_006343.2:c.584-98_584-96del	NP_006334.2:n.584-98_584-96del
XM_005263565.3:c.584-98_584-96del	XP_005263622.1:n.584-98_584-96del
XM_005263568.3:c.584-98_584-96del	XP_005263625.1:n.584-98_584-96del
XM_011510490.1:c.395-98_395-96del	XP_011508792.1:n.395-98_395-96del
XM_005263565.4:c.584-98_584-96del	XP_005263622.1:n.584-98_584-96del
XM_005263568.4:c.584-98_584-96del	XP_005263625.1:n.584-98_584-96del
XM_011510490.3:c.395-98_395-96del	XP_011508792.1:n.395-98_395-96del
XM_017003164.1:c.395-98_395-96del	XP_016858653.1:n.395-98_395-96del
XM_017003165.2:c.-684-98_-684-96del	XP_016858654.1:n.-684-98_-684-96del
NM_006343.3:c.584-98_584-96del MANE Select	NP_006334.2:n.584-98_584-96del