Canonical Allele Identifier: CA2751717334

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947633_111947634insAGA , CM000664.2:g.111947633_111947634insAGA	GRCh38
NC_000002.11:g.112705210_112705211insAGA , CM000664.1:g.112705210_112705211insAGA	GRCh37
NC_000002.10:g.112421681_112421682insAGA	NCBI36
NG_011607.1:g.54020_54021insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+66_757+67insAGA MANE Select	ENSP00000295408.4:n.757+66_757+67insAGA
ENST00000295408.8:c.757+66_757+67insAGA	ENSP00000295408.4:n.757+66_757+67insAGA
ENST00000409780.5:c.229+66_229+67insAGA	ENSP00000387277.1:n.229+66_229+67insAGA
ENST00000421804.6:c.757+66_757+67insAGA	ENSP00000389152.2:n.757+66_757+67insAGA
ENST00000439966.5:c.*230+66_*230+67insAGA	ENSP00000402129.1:n.*230+66_*230+67insAGA
ENST00000616902.4:c.-459+66_-459+67insAGA	ENSP00000482824.1:n.-459+66_-459+67insAGA
NM_006343.2:c.757+66_757+67insAGA	NP_006334.2:n.757+66_757+67insAGA
XM_005263565.3:c.757+66_757+67insAGA	XP_005263622.1:n.757+66_757+67insAGA
XM_005263568.3:c.757+66_757+67insAGA	XP_005263625.1:n.757+66_757+67insAGA
XM_011510490.1:c.568+66_568+67insAGA	XP_011508792.1:n.568+66_568+67insAGA
XM_005263565.4:c.757+66_757+67insAGA	XP_005263622.1:n.757+66_757+67insAGA
XM_005263568.4:c.757+66_757+67insAGA	XP_005263625.1:n.757+66_757+67insAGA
XM_011510490.3:c.568+66_568+67insAGA	XP_011508792.1:n.568+66_568+67insAGA
XM_017003164.1:c.568+66_568+67insAGA	XP_016858653.1:n.568+66_568+67insAGA
XM_017003165.2:c.-511+66_-511+67insAGA	XP_016858654.1:n.-511+66_-511+67insAGA
NM_006343.3:c.757+66_757+67insAGA MANE Select	NP_006334.2:n.757+66_757+67insAGA