Canonical Allele Identifier: CA348229217
Gene: MERTK HGNC NCBI

Linked Data

dbSNP Id: rs1163987038

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947514G>A , CM000664.2:g.111947514G>A GRCh38
NC_000002.11:g.112705091G>A , CM000664.1:g.112705091G>A GRCh37
NC_000002.10:g.112421562G>A NCBI36
NG_011607.1:g.53901G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.704G>A MANE Select ENSP00000295408.4:p.Ser235Asn
ENST00000295408.8:c.704G>A ENSP00000295408.4:p.Ser235Asn
ENST00000409780.5:c.176G>A ENSP00000387277.1:p.Ser59Asn
ENST00000421804.6:c.704G>A ENSP00000389152.2:p.Ser235Asn
ENST00000439966.5:c.*177G>A ENSP00000402129.1:n.*177G>A
ENST00000616902.4:c.-512G>A ENSP00000482824.1:n.-512G>A
NM_006343.2:c.704G>A NP_006334.2:p.Ser235Asn
XM_005263565.3:c.704G>A XP_005263622.1:p.Ser235Asn
XM_005263568.3:c.704G>A XP_005263625.1:p.Ser235Asn
XM_011510490.1:c.515G>A XP_011508792.1:p.Ser172Asn
XM_005263565.4:c.704G>A XP_005263622.1:p.Ser235Asn
XM_005263568.4:c.704G>A XP_005263625.1:p.Ser235Asn
XM_011510490.3:c.515G>A XP_011508792.1:p.Ser172Asn
XM_017003164.1:c.515G>A XP_016858653.1:p.Ser172Asn
XM_017003165.2:c.-564G>A XP_016858654.1:n.-564G>A
NM_006343.3:c.704G>A MANE Select NP_006334.2:p.Ser235Asn