Canonical Allele Identifier: CA348229023

Gene: MERTK

Linked Data

• dbSNP Id: rs1684979744
• MyVariant Identifiers: chr2:g.112705004T>C (hg19) ; chr2:g.111947427T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947427T>C , CM000664.2:g.111947427T>C	GRCh38
NC_000002.11:g.112705004T>C , CM000664.1:g.112705004T>C	GRCh37
NC_000002.10:g.112421475T>C	NCBI36
NG_011607.1:g.53814T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.617T>C MANE Select	ENSP00000295408.4:p.Met206Thr
ENST00000295408.8:c.617T>C	ENSP00000295408.4:p.Met206Thr
ENST00000409780.5:c.89T>C	ENSP00000387277.1:p.Met30Thr
ENST00000421804.6:c.617T>C	ENSP00000389152.2:p.Met206Thr
ENST00000439966.5:c.*90T>C	ENSP00000402129.1:n.*90T>C
ENST00000616902.4:c.-599T>C	ENSP00000482824.1:n.-599T>C
NM_006343.2:c.617T>C	NP_006334.2:p.Met206Thr
XM_005263565.3:c.617T>C	XP_005263622.1:p.Met206Thr
XM_005263568.3:c.617T>C	XP_005263625.1:p.Met206Thr
XM_011510490.1:c.428T>C	XP_011508792.1:p.Met143Thr
XM_005263565.4:c.617T>C	XP_005263622.1:p.Met206Thr
XM_005263568.4:c.617T>C	XP_005263625.1:p.Met206Thr
XM_011510490.3:c.428T>C	XP_011508792.1:p.Met143Thr
XM_017003164.1:c.428T>C	XP_016858653.1:p.Met143Thr
XM_017003165.2:c.-651T>C	XP_016858654.1:n.-651T>C
NM_006343.3:c.617T>C MANE Select	NP_006334.2:p.Met206Thr