Canonical Allele Identifier: CA1279566560

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997388T= , CM000664.2:g.111997388T=	GRCh38
NC_000002.11:g.112754965T= , CM000664.1:g.112754965T=	GRCh37
NC_000002.10:g.112471436T=	NCBI36
NG_011607.1:g.103775T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1516T= MANE Select	ENSP00000295408.4:p.Phe506=
ENST00000295408.8:c.1516T=	ENSP00000295408.4:p.Phe506=
ENST00000409780.5:c.988T=	ENSP00000387277.1:p.Phe330=
ENST00000421804.6:c.1516T=	ENSP00000389152.2:p.Phe506=
ENST00000439966.5:c.*989T=	ENSP00000402129.1:n.*989T=
ENST00000473065.1:n.19T=
ENST00000616902.4:c.485T=	ENSP00000482824.1:p.Leu162=
NM_006343.2:c.1516T=	NP_006334.2:p.Phe506=
XM_005263565.3:c.1516T=	XP_005263622.1:p.Phe506=
XM_005263568.3:c.1516T=	XP_005263625.1:p.Phe506=
XM_011510490.1:c.1327T=	XP_011508792.1:p.Phe443=
XM_011510491.1:c.301T=	XP_011508793.1:p.Phe101=
XM_005263565.4:c.1516T=	XP_005263622.1:p.Phe506=
XM_005263568.4:c.1516T=	XP_005263625.1:p.Phe506=
XM_011510490.3:c.1327T=	XP_011508792.1:p.Phe443=
XM_017003164.1:c.1327T=	XP_016858653.1:p.Phe443=
XM_017003165.2:c.301T=	XP_016858654.1:p.Phe101=
NM_006343.3:c.1516T= MANE Select	NP_006334.2:p.Phe506=