Canonical Allele Identifier: CA2751717331

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947632_111947636del , CM000664.2:g.111947632_111947636del	GRCh38
NC_000002.11:g.112705209_112705213del , CM000664.1:g.112705209_112705213del	GRCh37
NC_000002.10:g.112421680_112421684del	NCBI36
NG_011607.1:g.54019_54023del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+65_757+69del MANE Select	ENSP00000295408.4:n.757+65_757+69del
ENST00000295408.8:c.757+65_757+69del	ENSP00000295408.4:n.757+65_757+69del
ENST00000409780.5:c.229+65_229+69del	ENSP00000387277.1:n.229+65_229+69del
ENST00000421804.6:c.757+65_757+69del	ENSP00000389152.2:n.757+65_757+69del
ENST00000439966.5:c.*230+65_*230+69del	ENSP00000402129.1:n.*230+65_*230+69del
ENST00000616902.4:c.-459+65_-459+69del	ENSP00000482824.1:n.-459+65_-459+69del
NM_006343.2:c.757+65_757+69del	NP_006334.2:n.757+65_757+69del
XM_005263565.3:c.757+65_757+69del	XP_005263622.1:n.757+65_757+69del
XM_005263568.3:c.757+65_757+69del	XP_005263625.1:n.757+65_757+69del
XM_011510490.1:c.568+65_568+69del	XP_011508792.1:n.568+65_568+69del
XM_005263565.4:c.757+65_757+69del	XP_005263622.1:n.757+65_757+69del
XM_005263568.4:c.757+65_757+69del	XP_005263625.1:n.757+65_757+69del
XM_011510490.3:c.568+65_568+69del	XP_011508792.1:n.568+65_568+69del
XM_017003164.1:c.568+65_568+69del	XP_016858653.1:n.568+65_568+69del
XM_017003165.2:c.-511+65_-511+69del	XP_016858654.1:n.-511+65_-511+69del
NM_006343.3:c.757+65_757+69del MANE Select	NP_006334.2:n.757+65_757+69del