Canonical Allele Identifier: CA2751717343

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947638_111947639insT , CM000664.2:g.111947638_111947639insT	GRCh38
NC_000002.11:g.112705215_112705216insT , CM000664.1:g.112705215_112705216insT	GRCh37
NC_000002.10:g.112421686_112421687insT	NCBI36
NG_011607.1:g.54025_54026insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+71_757+72insT MANE Select	ENSP00000295408.4:n.757+71_757+72insT
ENST00000295408.8:c.757+71_757+72insT	ENSP00000295408.4:n.757+71_757+72insT
ENST00000409780.5:c.229+71_229+72insT	ENSP00000387277.1:n.229+71_229+72insT
ENST00000421804.6:c.757+71_757+72insT	ENSP00000389152.2:n.757+71_757+72insT
ENST00000439966.5:c.*230+71_*230+72insT	ENSP00000402129.1:n.*230+71_*230+72insT
ENST00000616902.4:c.-459+71_-459+72insT	ENSP00000482824.1:n.-459+71_-459+72insT
NM_006343.2:c.757+71_757+72insT	NP_006334.2:n.757+71_757+72insT
XM_005263565.3:c.757+71_757+72insT	XP_005263622.1:n.757+71_757+72insT
XM_005263568.3:c.757+71_757+72insT	XP_005263625.1:n.757+71_757+72insT
XM_011510490.1:c.568+71_568+72insT	XP_011508792.1:n.568+71_568+72insT
XM_005263565.4:c.757+71_757+72insT	XP_005263622.1:n.757+71_757+72insT
XM_005263568.4:c.757+71_757+72insT	XP_005263625.1:n.757+71_757+72insT
XM_011510490.3:c.568+71_568+72insT	XP_011508792.1:n.568+71_568+72insT
XM_017003164.1:c.568+71_568+72insT	XP_016858653.1:n.568+71_568+72insT
XM_017003165.2:c.-511+71_-511+72insT	XP_016858654.1:n.-511+71_-511+72insT
NM_006343.3:c.757+71_757+72insT MANE Select	NP_006334.2:n.757+71_757+72insT