Canonical Allele Identifier: CA348229174
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947498T>C , CM000664.2:g.111947498T>C GRCh38
NC_000002.11:g.112705075T>C , CM000664.1:g.112705075T>C GRCh37
NC_000002.10:g.112421546T>C NCBI36
NG_011607.1:g.53885T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.688T>C MANE Select ENSP00000295408.4:p.Phe230Leu
ENST00000295408.8:c.688T>C ENSP00000295408.4:p.Phe230Leu
ENST00000409780.5:c.160T>C ENSP00000387277.1:p.Phe54Leu
ENST00000421804.6:c.688T>C ENSP00000389152.2:p.Phe230Leu
ENST00000439966.5:c.*161T>C ENSP00000402129.1:n.*161T>C
ENST00000616902.4:c.-528T>C ENSP00000482824.1:n.-528T>C
NM_006343.2:c.688T>C NP_006334.2:p.Phe230Leu
XM_005263565.3:c.688T>C XP_005263622.1:p.Phe230Leu
XM_005263568.3:c.688T>C XP_005263625.1:p.Phe230Leu
XM_011510490.1:c.499T>C XP_011508792.1:p.Phe167Leu
XM_005263565.4:c.688T>C XP_005263622.1:p.Phe230Leu
XM_005263568.4:c.688T>C XP_005263625.1:p.Phe230Leu
XM_011510490.3:c.499T>C XP_011508792.1:p.Phe167Leu
XM_017003164.1:c.499T>C XP_016858653.1:p.Phe167Leu
XM_017003165.2:c.-580T>C XP_016858654.1:n.-580T>C
NM_006343.3:c.688T>C MANE Select NP_006334.2:p.Phe230Leu