Canonical Allele Identifier: CA348236872

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112019495A>C , CM000664.2:g.112019495A>C	GRCh38
NC_000002.11:g.112777072A>C , CM000664.1:g.112777072A>C	GRCh37
NC_000002.10:g.112493543A>C	NCBI36
NG_011607.1:g.125882A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.2162A>C MANE Select	ENSP00000295408.4:p.His721Pro
ENST00000295408.8:c.2162A>C	ENSP00000295408.4:p.His721Pro
ENST00000409780.5:c.1634A>C	ENSP00000387277.1:p.His545Pro
ENST00000421804.6:c.2162A>C	ENSP00000389152.2:p.His721Pro
ENST00000439966.5:c.*1635A>C	ENSP00000402129.1:n.*1635A>C
ENST00000449344.2:c.83A>C	ENSP00000412660.2:p.His28Pro
ENST00000616902.4:c.1118A>C	ENSP00000482824.1:p.His373Pro
NM_006343.2:c.2162A>C	NP_006334.2:p.His721Pro
XM_005263565.3:c.2162A>C	XP_005263622.1:p.His721Pro
XM_005263568.3:c.2162A>C	XP_005263625.1:p.His721Pro
XM_011510490.1:c.1973A>C	XP_011508792.1:p.His658Pro
XM_011510491.1:c.947A>C	XP_011508793.1:p.His316Pro
XM_005263565.4:c.2162A>C	XP_005263622.1:p.His721Pro
XM_005263568.4:c.2162A>C	XP_005263625.1:p.His721Pro
XM_011510490.3:c.1973A>C	XP_011508792.1:p.His658Pro
XM_017003164.1:c.1973A>C	XP_016858653.1:p.His658Pro
XM_017003165.2:c.947A>C	XP_016858654.1:p.His316Pro
NM_006343.3:c.2162A>C MANE Select	NP_006334.2:p.His721Pro