Canonical Allele Identifier: CA1279544383

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947623_111947624delinsAG , CM000664.2:g.111947623_111947624delinsAG	GRCh38
NC_000002.11:g.112705200_112705201delinsAG , CM000664.1:g.112705200_112705201delinsAG	GRCh37
NC_000002.10:g.112421671_112421672delinsAG	NCBI36
NG_011607.1:g.54010_54011delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+56_757+57delinsAG MANE Select	ENSP00000295408.4:n.757+56_757+57delinsAG
ENST00000295408.8:c.757+56_757+57delinsAG	ENSP00000295408.4:n.757+56_757+57delinsAG
ENST00000409780.5:c.229+56_229+57delinsAG	ENSP00000387277.1:n.229+56_229+57delinsAG
ENST00000421804.6:c.757+56_757+57delinsAG	ENSP00000389152.2:n.757+56_757+57delinsAG
ENST00000439966.5:c.*230+56_*230+57delinsAG	ENSP00000402129.1:n.*230+56_*230+57delinsAG
ENST00000616902.4:c.-459+56_-459+57delinsAG	ENSP00000482824.1:n.-459+56_-459+57delinsAG
NM_006343.2:c.757+56_757+57delinsAG	NP_006334.2:n.757+56_757+57delinsAG
XM_005263565.3:c.757+56_757+57delinsAG	XP_005263622.1:n.757+56_757+57delinsAG
XM_005263568.3:c.757+56_757+57delinsAG	XP_005263625.1:n.757+56_757+57delinsAG
XM_011510490.1:c.568+56_568+57delinsAG	XP_011508792.1:n.568+56_568+57delinsAG
XM_005263565.4:c.757+56_757+57delinsAG	XP_005263622.1:n.757+56_757+57delinsAG
XM_005263568.4:c.757+56_757+57delinsAG	XP_005263625.1:n.757+56_757+57delinsAG
XM_011510490.3:c.568+56_568+57delinsAG	XP_011508792.1:n.568+56_568+57delinsAG
XM_017003164.1:c.568+56_568+57delinsAG	XP_016858653.1:n.568+56_568+57delinsAG
XM_017003165.2:c.-511+56_-511+57delinsAG	XP_016858654.1:n.-511+56_-511+57delinsAG
NM_006343.3:c.757+56_757+57delinsAG MANE Select	NP_006334.2:n.757+56_757+57delinsAG