Canonical Allele Identifier: CA1279571260

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112008457A= , CM000664.2:g.112008457A=	GRCh38
NC_000002.11:g.112766034A= , CM000664.1:g.112766034A=	GRCh37
NC_000002.10:g.112482505A=	NCBI36
NG_011607.1:g.114844A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1942A= MANE Select	ENSP00000295408.4:p.Asn648=
ENST00000295408.8:c.1942A=	ENSP00000295408.4:p.Asn648=
ENST00000409780.5:c.1414A=	ENSP00000387277.1:p.Asn472=
ENST00000421804.6:c.1942A=	ENSP00000389152.2:p.Asn648=
ENST00000439966.5:c.*1415A=	ENSP00000402129.1:n.*1415A=
ENST00000616902.4:c.907A=	ENSP00000482824.1:p.Asn303=
NM_006343.2:c.1942A=	NP_006334.2:p.Asn648=
XM_005263565.3:c.1942A=	XP_005263622.1:p.Asn648=
XM_005263568.3:c.1942A=	XP_005263625.1:p.Asn648=
XM_011510490.1:c.1753A=	XP_011508792.1:p.Asn585=
XM_011510491.1:c.727A=	XP_011508793.1:p.Asn243=
XM_005263565.4:c.1942A=	XP_005263622.1:p.Asn648=
XM_005263568.4:c.1942A=	XP_005263625.1:p.Asn648=
XM_011510490.3:c.1753A=	XP_011508792.1:p.Asn585=
XM_017003164.1:c.1753A=	XP_016858653.1:p.Asn585=
XM_017003165.2:c.727A=	XP_016858654.1:p.Asn243=
NM_006343.3:c.1942A= MANE Select	NP_006334.2:p.Asn648=