Canonical Allele Identifier: CA2660687111

Gene: MERTK

Linked Data

• gnomAD v4: 2-111947302-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947302_111947303insAA , CM000664.2:g.111947302_111947303insAA	GRCh38
NC_000002.11:g.112704879_112704880insAA , CM000664.1:g.112704879_112704880insAA	GRCh37
NC_000002.10:g.112421350_112421351insAA	NCBI36
NG_011607.1:g.53689_53690insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.584-92_584-91insAA MANE Select	ENSP00000295408.4:n.584-92_584-91insAA
ENST00000295408.8:c.584-92_584-91insAA	ENSP00000295408.4:n.584-92_584-91insAA
ENST00000409780.5:c.56-92_56-91insAA	ENSP00000387277.1:n.56-92_56-91insAA
ENST00000421804.6:c.584-92_584-91insAA	ENSP00000389152.2:n.584-92_584-91insAA
ENST00000439966.5:c.*57-92_*57-91insAA	ENSP00000402129.1:n.*57-92_*57-91insAA
ENST00000616902.4:c.-632-92_-632-91insAA	ENSP00000482824.1:n.-632-92_-632-91insAA
NM_006343.2:c.584-92_584-91insAA	NP_006334.2:n.584-92_584-91insAA
XM_005263565.3:c.584-92_584-91insAA	XP_005263622.1:n.584-92_584-91insAA
XM_005263568.3:c.584-92_584-91insAA	XP_005263625.1:n.584-92_584-91insAA
XM_011510490.1:c.395-92_395-91insAA	XP_011508792.1:n.395-92_395-91insAA
XM_005263565.4:c.584-92_584-91insAA	XP_005263622.1:n.584-92_584-91insAA
XM_005263568.4:c.584-92_584-91insAA	XP_005263625.1:n.584-92_584-91insAA
XM_011510490.3:c.395-92_395-91insAA	XP_011508792.1:n.395-92_395-91insAA
XM_017003164.1:c.395-92_395-91insAA	XP_016858653.1:n.395-92_395-91insAA
XM_017003165.2:c.-684-92_-684-91insAA	XP_016858654.1:n.-684-92_-684-91insAA
NM_006343.3:c.584-92_584-91insAA MANE Select	NP_006334.2:n.584-92_584-91insAA