Canonical Allele Identifier: CA2751717377

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947695_111947701del , CM000664.2:g.111947695_111947701del	GRCh38
NC_000002.11:g.112705272_112705278del , CM000664.1:g.112705272_112705278del	GRCh37
NC_000002.10:g.112421743_112421749del	NCBI36
NG_011607.1:g.54082_54088del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+128_757+134del MANE Select	ENSP00000295408.4:n.757+128_757+134del
ENST00000295408.8:c.757+128_757+134del	ENSP00000295408.4:n.757+128_757+134del
ENST00000409780.5:c.229+128_229+134del	ENSP00000387277.1:n.229+128_229+134del
ENST00000421804.6:c.757+128_757+134del	ENSP00000389152.2:n.757+128_757+134del
ENST00000439966.5:c.*230+128_*230+134del	ENSP00000402129.1:n.*230+128_*230+134del
ENST00000616902.4:c.-459+128_-459+134del	ENSP00000482824.1:n.-459+128_-459+134del
NM_006343.2:c.757+128_757+134del	NP_006334.2:n.757+128_757+134del
XM_005263565.3:c.757+128_757+134del	XP_005263622.1:n.757+128_757+134del
XM_005263568.3:c.757+128_757+134del	XP_005263625.1:n.757+128_757+134del
XM_011510490.1:c.568+128_568+134del	XP_011508792.1:n.568+128_568+134del
XM_005263565.4:c.757+128_757+134del	XP_005263622.1:n.757+128_757+134del
XM_005263568.4:c.757+128_757+134del	XP_005263625.1:n.757+128_757+134del
XM_011510490.3:c.568+128_568+134del	XP_011508792.1:n.568+128_568+134del
XM_017003164.1:c.568+128_568+134del	XP_016858653.1:n.568+128_568+134del
XM_017003165.2:c.-511+128_-511+134del	XP_016858654.1:n.-511+128_-511+134del
NM_006343.3:c.757+128_757+134del MANE Select	NP_006334.2:n.757+128_757+134del