Canonical Allele Identifier: CA348229132
Gene: MERTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947477C>T , CM000664.2:g.111947477C>T GRCh38
NC_000002.11:g.112705054C>T , CM000664.1:g.112705054C>T GRCh37
NC_000002.10:g.112421525C>T NCBI36
NG_011607.1:g.53864C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.667C>T MANE Select ENSP00000295408.4:p.Pro223Ser
ENST00000295408.8:c.667C>T ENSP00000295408.4:p.Pro223Ser
ENST00000409780.5:c.139C>T ENSP00000387277.1:p.Pro47Ser
ENST00000421804.6:c.667C>T ENSP00000389152.2:p.Pro223Ser
ENST00000439966.5:c.*140C>T ENSP00000402129.1:n.*140C>T
ENST00000616902.4:c.-549C>T ENSP00000482824.1:n.-549C>T
NM_006343.2:c.667C>T NP_006334.2:p.Pro223Ser
XM_005263565.3:c.667C>T XP_005263622.1:p.Pro223Ser
XM_005263568.3:c.667C>T XP_005263625.1:p.Pro223Ser
XM_011510490.1:c.478C>T XP_011508792.1:p.Pro160Ser
XM_005263565.4:c.667C>T XP_005263622.1:p.Pro223Ser
XM_005263568.4:c.667C>T XP_005263625.1:p.Pro223Ser
XM_011510490.3:c.478C>T XP_011508792.1:p.Pro160Ser
XM_017003164.1:c.478C>T XP_016858653.1:p.Pro160Ser
XM_017003165.2:c.-601C>T XP_016858654.1:n.-601C>T
NM_006343.3:c.667C>T MANE Select NP_006334.2:p.Pro223Ser