Canonical Allele Identifier: CA1279536542

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111929509G= , CM000664.2:g.111929509G=	GRCh38
NC_000002.11:g.112687086G= , CM000664.1:g.112687086G=	GRCh37
NC_000002.10:g.112403557G=	NCBI36
NG_011607.1:g.35896G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.451G= MANE Select	ENSP00000295408.4:p.Asp151=
ENST00000295408.8:c.451G=	ENSP00000295408.4:p.Asp151=
ENST00000409780.5:c.-46-15451G=	ENSP00000387277.1:n.-46-15451G=
ENST00000421804.6:c.451G=	ENSP00000389152.2:p.Asp151=
ENST00000439966.5:c.246+205G=	ENSP00000402129.1:n.246+205G=
ENST00000616902.4:c.-765G=	ENSP00000482824.1:n.-765G=
NM_006343.2:c.451G=	NP_006334.2:p.Asp151=
XM_005263565.3:c.451G=	XP_005263622.1:p.Asp151=
XM_005263568.3:c.451G=	XP_005263625.1:p.Asp151=
XM_011510490.1:c.262G=	XP_011508792.1:p.Asp88=
XM_005263565.4:c.451G=	XP_005263622.1:p.Asp151=
XM_005263568.4:c.451G=	XP_005263625.1:p.Asp151=
XM_011510490.3:c.262G=	XP_011508792.1:p.Asp88=
XM_017003164.1:c.262G=	XP_016858653.1:p.Asp88=
XM_017003165.2:c.-817G=	XP_016858654.1:n.-817G=
NM_006343.3:c.451G= MANE Select	NP_006334.2:p.Asp151=