Canonical Allele Identifier: CA2697551015

Gene: MERTK

Linked Data

• ClinVar Variation Id: 2746270
• ClinVar RCV Id: RCV003562996

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947461_111947462delinsTG , CM000664.2:g.111947461_111947462delinsTG	GRCh38
NC_000002.11:g.112705038_112705039delinsTG , CM000664.1:g.112705038_112705039delinsTG	GRCh37
NC_000002.10:g.112421509_112421510delinsTG	NCBI36
NG_011607.1:g.53848_53849delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.651_652delinsTG MANE Select	ENSP00000295408.4:p.Cys218Gly
ENST00000295408.8:c.651_652delinsTG	ENSP00000295408.4:p.Cys218Gly
ENST00000409780.5:c.123_124delinsTG	ENSP00000387277.1:p.Cys42Gly
ENST00000421804.6:c.651_652delinsTG	ENSP00000389152.2:p.Cys218Gly
ENST00000439966.5:c.*124_*125delinsTG	ENSP00000402129.1:n.*124_*125delinsTG
ENST00000616902.4:c.-565_-564delinsTG	ENSP00000482824.1:n.-565_-564delinsTG
NM_006343.2:c.651_652delinsTG	NP_006334.2:p.Cys218Gly
XM_005263565.3:c.651_652delinsTG	XP_005263622.1:p.Cys218Gly
XM_005263568.3:c.651_652delinsTG	XP_005263625.1:p.Cys218Gly
XM_011510490.1:c.462_463delinsTG	XP_011508792.1:p.Cys155Gly
XM_005263565.4:c.651_652delinsTG	XP_005263622.1:p.Cys218Gly
XM_005263568.4:c.651_652delinsTG	XP_005263625.1:p.Cys218Gly
XM_011510490.3:c.462_463delinsTG	XP_011508792.1:p.Cys155Gly
XM_017003164.1:c.462_463delinsTG	XP_016858653.1:p.Cys155Gly
XM_017003165.2:c.-617_-616delinsTG	XP_016858654.1:n.-617_-616delinsTG
NM_006343.3:c.651_652delinsTG MANE Select	NP_006334.2:p.Cys218Gly