Canonical Allele Identifier: CA2660687112

Gene: MERTK

Linked Data

• gnomAD v4: 2-111947302-TTGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947303_111947305del , CM000664.2:g.111947303_111947305del	GRCh38
NC_000002.11:g.112704880_112704882del , CM000664.1:g.112704880_112704882del	GRCh37
NC_000002.10:g.112421351_112421353del	NCBI36
NG_011607.1:g.53690_53692del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.584-91_584-89del MANE Select	ENSP00000295408.4:n.584-91_584-89del
ENST00000295408.8:c.584-91_584-89del	ENSP00000295408.4:n.584-91_584-89del
ENST00000409780.5:c.56-91_56-89del	ENSP00000387277.1:n.56-91_56-89del
ENST00000421804.6:c.584-91_584-89del	ENSP00000389152.2:n.584-91_584-89del
ENST00000439966.5:c.*57-91_*57-89del	ENSP00000402129.1:n.*57-91_*57-89del
ENST00000616902.4:c.-632-91_-632-89del	ENSP00000482824.1:n.-632-91_-632-89del
NM_006343.2:c.584-91_584-89del	NP_006334.2:n.584-91_584-89del
XM_005263565.3:c.584-91_584-89del	XP_005263622.1:n.584-91_584-89del
XM_005263568.3:c.584-91_584-89del	XP_005263625.1:n.584-91_584-89del
XM_011510490.1:c.395-91_395-89del	XP_011508792.1:n.395-91_395-89del
XM_005263565.4:c.584-91_584-89del	XP_005263622.1:n.584-91_584-89del
XM_005263568.4:c.584-91_584-89del	XP_005263625.1:n.584-91_584-89del
XM_011510490.3:c.395-91_395-89del	XP_011508792.1:n.395-91_395-89del
XM_017003164.1:c.395-91_395-89del	XP_016858653.1:n.395-91_395-89del
XM_017003165.2:c.-684-91_-684-89del	XP_016858654.1:n.-684-91_-684-89del
NM_006343.3:c.584-91_584-89del MANE Select	NP_006334.2:n.584-91_584-89del