Canonical Allele Identifier: CA53591319

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112021426C>T , CM000664.2:g.112021426C>T	GRCh38
NC_000002.11:g.112779003C>T , CM000664.1:g.112779003C>T	GRCh37
NC_000002.10:g.112495474C>T	NCBI36
NG_011607.1:g.127813C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006343.3:c.2194C>T MANE Select	NP_006334.2:p.Arg732Ter
ENST00000295408.9:c.2194C>T MANE Select	ENSP00000295408.4:p.Arg732Ter
NM_006343.2:c.2194C>T	NP_006334.2:p.Arg732Ter
ENST00000295408.8:c.2194C>T	ENSP00000295408.4:p.Arg732Ter
ENST00000409780.5:c.1666C>T	ENSP00000387277.1:p.Arg556Ter
ENST00000421804.6:c.2194C>T	ENSP00000389152.2:p.Arg732Ter
ENST00000439966.5:c.*1667C>T	ENSP00000402129.1:n.*1667C>T
ENST00000449344.2:c.166C>T	ENSP00000412660.2:p.Arg56Ter
ENST00000616902.4:c.1150C>T	ENSP00000482824.1:p.Arg384Ter
XM_005263565.3:c.2194C>T	XP_005263622.1:p.Arg732Ter
XM_005263565.4:c.2194C>T	XP_005263622.1:p.Arg732Ter
XM_005263568.3:c.*50C>T	XP_005263625.1:n.*50C>T
XM_011510490.1:c.2005C>T	XP_011508792.1:p.Arg669Ter
XM_011510490.3:c.2005C>T	XP_011508792.1:p.Arg669Ter
XM_011510491.1:c.979C>T	XP_011508793.1:p.Arg327Ter
XM_017003164.1:c.2005C>T	XP_016858653.1:p.Arg669Ter
XM_017003165.2:c.979C>T	XP_016858654.1:p.Arg327Ter