Canonical Allele Identifier: CA658653751

Gene: MERTK

Linked Data

• ClinVar Variation Id: 444513
• ClinVar RCV Id: RCV000513363 ; RCV001199707
• dbSNP Id: rs1553452169

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111965279dup , CM000664.2:g.111965279dup	GRCh38
NC_000002.11:g.112722856dup , CM000664.1:g.112722856dup	GRCh37
NC_000002.10:g.112439327dup	NCBI36
NG_011607.1:g.71666dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.844+2dup MANE Select	ENSP00000295408.4:n.844+2dup
ENST00000295408.8:c.844+2dup	ENSP00000295408.4:n.844+2dup
ENST00000409780.5:c.316+2dup	ENSP00000387277.1:n.316+2dup
ENST00000421804.6:c.844+2dup	ENSP00000389152.2:n.844+2dup
ENST00000439966.5:c.*317+2dup	ENSP00000402129.1:n.*317+2dup
ENST00000616902.4:c.-372+2dup	ENSP00000482824.1:n.-372+2dup
NM_006343.2:c.844+2dup	NP_006334.2:n.844+2dup
XM_005263565.3:c.844+2dup	XP_005263622.1:n.844+2dup
XM_005263568.3:c.844+2dup	XP_005263625.1:n.844+2dup
XM_011510490.1:c.655+2dup	XP_011508792.1:n.655+2dup
XM_005263565.4:c.844+2dup	XP_005263622.1:n.844+2dup
XM_005263568.4:c.844+2dup	XP_005263625.1:n.844+2dup
XM_011510490.3:c.655+2dup	XP_011508792.1:n.655+2dup
XM_017003164.1:c.655+2dup	XP_016858653.1:n.655+2dup
XM_017003165.2:c.-424+2dup	XP_016858654.1:n.-424+2dup
NM_006343.3:c.844+2dup MANE Select	NP_006334.2:n.844+2dup