Canonical Allele Identifier: CA2751717266

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947552_111947553insACA , CM000664.2:g.111947552_111947553insACA	GRCh38
NC_000002.11:g.112705129_112705130insACA , CM000664.1:g.112705129_112705130insACA	GRCh37
NC_000002.10:g.112421600_112421601insACA	NCBI36
NG_011607.1:g.53939_53940insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.742_743insACA MANE Select	ENSP00000295408.4:p.Val248delinsAspMet
ENST00000295408.8:c.742_743insACA	ENSP00000295408.4:p.Val248delinsAspMet
ENST00000409780.5:c.214_215insACA	ENSP00000387277.1:p.Val72delinsAspMet
ENST00000421804.6:c.742_743insACA	ENSP00000389152.2:p.Val248delinsAspMet
ENST00000439966.5:c.*215_*216insACA	ENSP00000402129.1:n.*215_*216insACA
ENST00000616902.4:c.-474_-473insACA	ENSP00000482824.1:n.-474_-473insACA
NM_006343.2:c.742_743insACA	NP_006334.2:p.Val248delinsAspMet
XM_005263565.3:c.742_743insACA	XP_005263622.1:p.Val248delinsAspMet
XM_005263568.3:c.742_743insACA	XP_005263625.1:p.Val248delinsAspMet
XM_011510490.1:c.553_554insACA	XP_011508792.1:p.Val185delinsAspMet
XM_005263565.4:c.742_743insACA	XP_005263622.1:p.Val248delinsAspMet
XM_005263568.4:c.742_743insACA	XP_005263625.1:p.Val248delinsAspMet
XM_011510490.3:c.553_554insACA	XP_011508792.1:p.Val185delinsAspMet
XM_017003164.1:c.553_554insACA	XP_016858653.1:p.Val185delinsAspMet
XM_017003165.2:c.-526_-525insACA	XP_016858654.1:n.-526_-525insACA
NM_006343.3:c.742_743insACA MANE Select	NP_006334.2:p.Val248delinsAspMet