Canonical Allele Identifier: CA2751717360

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947669_111947670insG , CM000664.2:g.111947669_111947670insG	GRCh38
NC_000002.11:g.112705246_112705247insG , CM000664.1:g.112705246_112705247insG	GRCh37
NC_000002.10:g.112421717_112421718insG	NCBI36
NG_011607.1:g.54056_54057insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+102_757+103insG MANE Select	ENSP00000295408.4:n.757+102_757+103insG
ENST00000295408.8:c.757+102_757+103insG	ENSP00000295408.4:n.757+102_757+103insG
ENST00000409780.5:c.229+102_229+103insG	ENSP00000387277.1:n.229+102_229+103insG
ENST00000421804.6:c.757+102_757+103insG	ENSP00000389152.2:n.757+102_757+103insG
ENST00000439966.5:c.*230+102_*230+103insG	ENSP00000402129.1:n.*230+102_*230+103insG
ENST00000616902.4:c.-459+102_-459+103insG	ENSP00000482824.1:n.-459+102_-459+103insG
NM_006343.2:c.757+102_757+103insG	NP_006334.2:n.757+102_757+103insG
XM_005263565.3:c.757+102_757+103insG	XP_005263622.1:n.757+102_757+103insG
XM_005263568.3:c.757+102_757+103insG	XP_005263625.1:n.757+102_757+103insG
XM_011510490.1:c.568+102_568+103insG	XP_011508792.1:n.568+102_568+103insG
XM_005263565.4:c.757+102_757+103insG	XP_005263622.1:n.757+102_757+103insG
XM_005263568.4:c.757+102_757+103insG	XP_005263625.1:n.757+102_757+103insG
XM_011510490.3:c.568+102_568+103insG	XP_011508792.1:n.568+102_568+103insG
XM_017003164.1:c.568+102_568+103insG	XP_016858653.1:n.568+102_568+103insG
XM_017003165.2:c.-511+102_-511+103insG	XP_016858654.1:n.-511+102_-511+103insG
NM_006343.3:c.757+102_757+103insG MANE Select	NP_006334.2:n.757+102_757+103insG