Canonical Allele Identifier: CA2751717282

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947579_111947580insCAG , CM000664.2:g.111947579_111947580insCAG	GRCh38
NC_000002.11:g.112705156_112705157insCAG , CM000664.1:g.112705156_112705157insCAG	GRCh37
NC_000002.10:g.112421627_112421628insCAG	NCBI36
NG_011607.1:g.53966_53967insCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+12_757+13insCAG MANE Select	ENSP00000295408.4:n.757+12_757+13insCAG
ENST00000295408.8:c.757+12_757+13insCAG	ENSP00000295408.4:n.757+12_757+13insCAG
ENST00000409780.5:c.229+12_229+13insCAG	ENSP00000387277.1:n.229+12_229+13insCAG
ENST00000421804.6:c.757+12_757+13insCAG	ENSP00000389152.2:n.757+12_757+13insCAG
ENST00000439966.5:c.*230+12_*230+13insCAG	ENSP00000402129.1:n.*230+12_*230+13insCAG
ENST00000616902.4:c.-459+12_-459+13insCAG	ENSP00000482824.1:n.-459+12_-459+13insCAG
NM_006343.2:c.757+12_757+13insCAG	NP_006334.2:n.757+12_757+13insCAG
XM_005263565.3:c.757+12_757+13insCAG	XP_005263622.1:n.757+12_757+13insCAG
XM_005263568.3:c.757+12_757+13insCAG	XP_005263625.1:n.757+12_757+13insCAG
XM_011510490.1:c.568+12_568+13insCAG	XP_011508792.1:n.568+12_568+13insCAG
XM_005263565.4:c.757+12_757+13insCAG	XP_005263622.1:n.757+12_757+13insCAG
XM_005263568.4:c.757+12_757+13insCAG	XP_005263625.1:n.757+12_757+13insCAG
XM_011510490.3:c.568+12_568+13insCAG	XP_011508792.1:n.568+12_568+13insCAG
XM_017003164.1:c.568+12_568+13insCAG	XP_016858653.1:n.568+12_568+13insCAG
XM_017003165.2:c.-511+12_-511+13insCAG	XP_016858654.1:n.-511+12_-511+13insCAG
NM_006343.3:c.757+12_757+13insCAG MANE Select	NP_006334.2:n.757+12_757+13insCAG