Canonical Allele Identifier: CA428270379

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112705095C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947518C>T , CM000664.2:g.111947518C>T	GRCh38
NC_000002.11:g.112705095C>T , CM000664.1:g.112705095C>T	GRCh37
NC_000002.10:g.112421566C>T	NCBI36
NG_011607.1:g.53905C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.708C>T MANE Select	ENSP00000295408.4:p.Ser236=
ENST00000295408.8:c.708C>T	ENSP00000295408.4:p.Ser236=
ENST00000409780.5:c.180C>T	ENSP00000387277.1:p.Ser60=
ENST00000421804.6:c.708C>T	ENSP00000389152.2:p.Ser236=
ENST00000439966.5:c.*181C>T	ENSP00000402129.1:n.*181C>T
ENST00000616902.4:c.-508C>T	ENSP00000482824.1:n.-508C>T
NM_006343.2:c.708C>T	NP_006334.2:p.Ser236=
XM_005263565.3:c.708C>T	XP_005263622.1:p.Ser236=
XM_005263568.3:c.708C>T	XP_005263625.1:p.Ser236=
XM_011510490.1:c.519C>T	XP_011508792.1:p.Ser173=
XM_005263565.4:c.708C>T	XP_005263622.1:p.Ser236=
XM_005263568.4:c.708C>T	XP_005263625.1:p.Ser236=
XM_011510490.3:c.519C>T	XP_011508792.1:p.Ser173=
XM_017003164.1:c.519C>T	XP_016858653.1:p.Ser173=
XM_017003165.2:c.-560C>T	XP_016858654.1:n.-560C>T
NM_006343.3:c.708C>T MANE Select	NP_006334.2:p.Ser236=