Canonical Allele Identifier: CA2751719959

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112008589_112008590insC , CM000664.2:g.112008589_112008590insC	GRCh38
NC_000002.11:g.112766166_112766167insC , CM000664.1:g.112766166_112766167insC	GRCh37
NC_000002.10:g.112482637_112482638insC	NCBI36
NG_011607.1:g.114976_114977insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1960+114_1960+115insC MANE Select	ENSP00000295408.4:n.1960+114_1960+115insC
ENST00000295408.8:c.1960+114_1960+115insC	ENSP00000295408.4:n.1960+114_1960+115insC
ENST00000409780.5:c.1432+114_1432+115insC	ENSP00000387277.1:n.1432+114_1432+115insC
ENST00000421804.6:c.1960+114_1960+115insC	ENSP00000389152.2:n.1960+114_1960+115insC
ENST00000439966.5:c.*1433+114_*1433+115insC	ENSP00000402129.1:n.*1433+114_*1433+115insC
ENST00000616902.4:c.925+114_925+115insC	ENSP00000482824.1:n.925+114_925+115insC
NM_006343.2:c.1960+114_1960+115insC	NP_006334.2:n.1960+114_1960+115insC
XM_005263565.3:c.1960+114_1960+115insC	XP_005263622.1:n.1960+114_1960+115insC
XM_005263568.3:c.1960+114_1960+115insC	XP_005263625.1:n.1960+114_1960+115insC
XM_011510490.1:c.1771+114_1771+115insC	XP_011508792.1:n.1771+114_1771+115insC
XM_011510491.1:c.745+114_745+115insC	XP_011508793.1:n.745+114_745+115insC
XM_005263565.4:c.1960+114_1960+115insC	XP_005263622.1:n.1960+114_1960+115insC
XM_005263568.4:c.1960+114_1960+115insC	XP_005263625.1:n.1960+114_1960+115insC
XM_011510490.3:c.1771+114_1771+115insC	XP_011508792.1:n.1771+114_1771+115insC
XM_017003164.1:c.1771+114_1771+115insC	XP_016858653.1:n.1771+114_1771+115insC
XM_017003165.2:c.745+114_745+115insC	XP_016858654.1:n.745+114_745+115insC
NM_006343.3:c.1960+114_1960+115insC MANE Select	NP_006334.2:n.1960+114_1960+115insC