Canonical Allele Identifier: CA2751717387

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947735_111947747del , CM000664.2:g.111947735_111947747del	GRCh38
NC_000002.11:g.112705312_112705324del , CM000664.1:g.112705312_112705324del	GRCh37
NC_000002.10:g.112421783_112421795del	NCBI36
NG_011607.1:g.54122_54134del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+168_757+180del MANE Select	ENSP00000295408.4:n.757+168_757+180del
ENST00000295408.8:c.757+168_757+180del	ENSP00000295408.4:n.757+168_757+180del
ENST00000409780.5:c.229+168_229+180del	ENSP00000387277.1:n.229+168_229+180del
ENST00000421804.6:c.757+168_757+180del	ENSP00000389152.2:n.757+168_757+180del
ENST00000439966.5:c.*230+168_*230+180del	ENSP00000402129.1:n.*230+168_*230+180del
ENST00000616902.4:c.-459+168_-459+180del	ENSP00000482824.1:n.-459+168_-459+180del
NM_006343.2:c.757+168_757+180del	NP_006334.2:n.757+168_757+180del
XM_005263565.3:c.757+168_757+180del	XP_005263622.1:n.757+168_757+180del
XM_005263568.3:c.757+168_757+180del	XP_005263625.1:n.757+168_757+180del
XM_011510490.1:c.568+168_568+180del	XP_011508792.1:n.568+168_568+180del
XM_005263565.4:c.757+168_757+180del	XP_005263622.1:n.757+168_757+180del
XM_005263568.4:c.757+168_757+180del	XP_005263625.1:n.757+168_757+180del
XM_011510490.3:c.568+168_568+180del	XP_011508792.1:n.568+168_568+180del
XM_017003164.1:c.568+168_568+180del	XP_016858653.1:n.568+168_568+180del
XM_017003165.2:c.-511+168_-511+180del	XP_016858654.1:n.-511+168_-511+180del
NM_006343.3:c.757+168_757+180del MANE Select	NP_006334.2:n.757+168_757+180del