Canonical Allele Identifier: CA1279544322

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947488C= , CM000664.2:g.111947488C=	GRCh38
NC_000002.11:g.112705065C= , CM000664.1:g.112705065C=	GRCh37
NC_000002.10:g.112421536C=	NCBI36
NG_011607.1:g.53875C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.678C= MANE Select	ENSP00000295408.4:p.Pro226=
ENST00000295408.8:c.678C=	ENSP00000295408.4:p.Pro226=
ENST00000409780.5:c.150C=	ENSP00000387277.1:p.Pro50=
ENST00000421804.6:c.678C=	ENSP00000389152.2:p.Pro226=
ENST00000439966.5:c.*151C=	ENSP00000402129.1:n.*151C=
ENST00000616902.4:c.-538C=	ENSP00000482824.1:n.-538C=
NM_006343.2:c.678C=	NP_006334.2:p.Pro226=
XM_005263565.3:c.678C=	XP_005263622.1:p.Pro226=
XM_005263568.3:c.678C=	XP_005263625.1:p.Pro226=
XM_011510490.1:c.489C=	XP_011508792.1:p.Pro163=
XM_005263565.4:c.678C=	XP_005263622.1:p.Pro226=
XM_005263568.4:c.678C=	XP_005263625.1:p.Pro226=
XM_011510490.3:c.489C=	XP_011508792.1:p.Pro163=
XM_017003164.1:c.489C=	XP_016858653.1:p.Pro163=
XM_017003165.2:c.-590C=	XP_016858654.1:n.-590C=
NM_006343.3:c.678C= MANE Select	NP_006334.2:p.Pro226=