Canonical Allele Identifier: CA348231355

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112754975T>C (hg19) ; chr2:g.111997398T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997398T>C , CM000664.2:g.111997398T>C	GRCh38
NC_000002.11:g.112754975T>C , CM000664.1:g.112754975T>C	GRCh37
NC_000002.10:g.112471446T>C	NCBI36
NG_011607.1:g.103785T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1526T>C MANE Select	ENSP00000295408.4:p.Phe509Ser
ENST00000295408.8:c.1526T>C	ENSP00000295408.4:p.Phe509Ser
ENST00000409780.5:c.998T>C	ENSP00000387277.1:p.Phe333Ser
ENST00000421804.6:c.1526T>C	ENSP00000389152.2:p.Phe509Ser
ENST00000439966.5:c.*999T>C	ENSP00000402129.1:n.*999T>C
ENST00000473065.1:n.29T>C
ENST00000616902.4:c.495T>C	ENSP00000482824.1:p.Leu165=
NM_006343.2:c.1526T>C	NP_006334.2:p.Phe509Ser
XM_005263565.3:c.1526T>C	XP_005263622.1:p.Phe509Ser
XM_005263568.3:c.1526T>C	XP_005263625.1:p.Phe509Ser
XM_011510490.1:c.1337T>C	XP_011508792.1:p.Phe446Ser
XM_011510491.1:c.311T>C	XP_011508793.1:p.Phe104Ser
XM_005263565.4:c.1526T>C	XP_005263622.1:p.Phe509Ser
XM_005263568.4:c.1526T>C	XP_005263625.1:p.Phe509Ser
XM_011510490.3:c.1337T>C	XP_011508792.1:p.Phe446Ser
XM_017003164.1:c.1337T>C	XP_016858653.1:p.Phe446Ser
XM_017003165.2:c.311T>C	XP_016858654.1:p.Phe104Ser
NM_006343.3:c.1526T>C MANE Select	NP_006334.2:p.Phe509Ser