Canonical Allele Identifier: CA1279544357

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947566A= , CM000664.2:g.111947566A=	GRCh38
NC_000002.11:g.112705143A= , CM000664.1:g.112705143A=	GRCh37
NC_000002.10:g.112421614A=	NCBI36
NG_011607.1:g.53953A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.756A= MANE Select	ENSP00000295408.4:p.Pro252=
ENST00000295408.8:c.756A=	ENSP00000295408.4:p.Pro252=
ENST00000409780.5:c.228A=	ENSP00000387277.1:p.Pro76=
ENST00000421804.6:c.756A=	ENSP00000389152.2:p.Pro252=
ENST00000439966.5:c.*229A=	ENSP00000402129.1:n.*229A=
ENST00000616902.4:c.-460A=	ENSP00000482824.1:n.-460A=
NM_006343.2:c.756A=	NP_006334.2:p.Pro252=
XM_005263565.3:c.756A=	XP_005263622.1:p.Pro252=
XM_005263568.3:c.756A=	XP_005263625.1:p.Pro252=
XM_011510490.1:c.567A=	XP_011508792.1:p.Pro189=
XM_005263565.4:c.756A=	XP_005263622.1:p.Pro252=
XM_005263568.4:c.756A=	XP_005263625.1:p.Pro252=
XM_011510490.3:c.567A=	XP_011508792.1:p.Pro189=
XM_017003164.1:c.567A=	XP_016858653.1:p.Pro189=
XM_017003165.2:c.-512A=	XP_016858654.1:n.-512A=
NM_006343.3:c.756A= MANE Select	NP_006334.2:p.Pro252=