Canonical Allele Identifier: CA2580063750
Gene: MERTK HGNC NCBI

Linked Data

ClinVar Variation Id: 1992796
ClinVar RCV Id: RCV002796188

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947393_111947394dup , CM000664.2:g.111947393_111947394dup GRCh38
NC_000002.11:g.112704970_112704971dup , CM000664.1:g.112704970_112704971dup GRCh37
NC_000002.10:g.112421441_112421442dup NCBI36
NG_011607.1:g.53780_53781dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.584-1_584dup
ENST00000295408.8:c.584-1_584dup
ENST00000409780.5:c.56-1_56dup
ENST00000421804.6:c.584-1_584dup
ENST00000439966.5:c.*57-1_*57dup
ENST00000616902.4:c.-632-1_-632dup
NM_006343.2:c.584-1_584dup
XM_005263565.3:c.584-1_584dup
XM_005263568.3:c.584-1_584dup
XM_011510490.1:c.395-1_395dup
XM_005263565.4:c.584-1_584dup
XM_005263568.4:c.584-1_584dup
XM_011510490.3:c.395-1_395dup
XM_017003164.1:c.395-1_395dup
XM_017003165.2:c.-684-1_-684dup
NM_006343.3:c.584-1_584dup