Canonical Allele Identifier: CA2751717321

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947626_111947627insACA , CM000664.2:g.111947626_111947627insACA	GRCh38
NC_000002.11:g.112705203_112705204insACA , CM000664.1:g.112705203_112705204insACA	GRCh37
NC_000002.10:g.112421674_112421675insACA	NCBI36
NG_011607.1:g.54013_54014insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+59_757+60insACA MANE Select	ENSP00000295408.4:n.757+59_757+60insACA
ENST00000295408.8:c.757+59_757+60insACA	ENSP00000295408.4:n.757+59_757+60insACA
ENST00000409780.5:c.229+59_229+60insACA	ENSP00000387277.1:n.229+59_229+60insACA
ENST00000421804.6:c.757+59_757+60insACA	ENSP00000389152.2:n.757+59_757+60insACA
ENST00000439966.5:c.*230+59_*230+60insACA	ENSP00000402129.1:n.*230+59_*230+60insACA
ENST00000616902.4:c.-459+59_-459+60insACA	ENSP00000482824.1:n.-459+59_-459+60insACA
NM_006343.2:c.757+59_757+60insACA	NP_006334.2:n.757+59_757+60insACA
XM_005263565.3:c.757+59_757+60insACA	XP_005263622.1:n.757+59_757+60insACA
XM_005263568.3:c.757+59_757+60insACA	XP_005263625.1:n.757+59_757+60insACA
XM_011510490.1:c.568+59_568+60insACA	XP_011508792.1:n.568+59_568+60insACA
XM_005263565.4:c.757+59_757+60insACA	XP_005263622.1:n.757+59_757+60insACA
XM_005263568.4:c.757+59_757+60insACA	XP_005263625.1:n.757+59_757+60insACA
XM_011510490.3:c.568+59_568+60insACA	XP_011508792.1:n.568+59_568+60insACA
XM_017003164.1:c.568+59_568+60insACA	XP_016858653.1:n.568+59_568+60insACA
XM_017003165.2:c.-511+59_-511+60insACA	XP_016858654.1:n.-511+59_-511+60insACA
NM_006343.3:c.757+59_757+60insACA MANE Select	NP_006334.2:n.757+59_757+60insACA