Canonical Allele Identifier: CA348226471

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112686987A>C (hg19) ; chr2:g.111929410A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111929410A>C , CM000664.2:g.111929410A>C	GRCh38
NC_000002.11:g.112686987A>C , CM000664.1:g.112686987A>C	GRCh37
NC_000002.10:g.112403458A>C	NCBI36
NG_011607.1:g.35797A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.352A>C MANE Select	ENSP00000295408.4:p.Ser118Arg
ENST00000295408.8:c.352A>C	ENSP00000295408.4:p.Ser118Arg
ENST00000409780.5:c.-46-15550A>C	ENSP00000387277.1:n.-46-15550A>C
ENST00000421804.6:c.352A>C	ENSP00000389152.2:p.Ser118Arg
ENST00000439966.5:c.246+106A>C	ENSP00000402129.1:n.246+106A>C
ENST00000616902.4:c.-864A>C	ENSP00000482824.1:n.-864A>C
NM_006343.2:c.352A>C	NP_006334.2:p.Ser118Arg
XM_005263565.3:c.352A>C	XP_005263622.1:p.Ser118Arg
XM_005263568.3:c.352A>C	XP_005263625.1:p.Ser118Arg
XM_011510490.1:c.163A>C	XP_011508792.1:p.Ser55Arg
XM_005263565.4:c.352A>C	XP_005263622.1:p.Ser118Arg
XM_005263568.4:c.352A>C	XP_005263625.1:p.Ser118Arg
XM_011510490.3:c.163A>C	XP_011508792.1:p.Ser55Arg
XM_017003164.1:c.163A>C	XP_016858653.1:p.Ser55Arg
XM_017003165.2:c.-916A>C	XP_016858654.1:n.-916A>C
NM_006343.3:c.352A>C MANE Select	NP_006334.2:p.Ser118Arg