Canonical Allele Identifier: CA1279544329

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947507_111947509delinsCAA , CM000664.2:g.111947507_111947509delinsCAA	GRCh38
NC_000002.11:g.112705084_112705086delinsCAA , CM000664.1:g.112705084_112705086delinsCAA	GRCh37
NC_000002.10:g.112421555_112421557delinsCAA	NCBI36
NG_011607.1:g.53894_53896delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.697_699delinsCAA MANE Select	ENSP00000295408.4:p.Gln233=
ENST00000295408.8:c.697_699delinsCAA	ENSP00000295408.4:p.Gln233=
ENST00000409780.5:c.169_171delinsCAA	ENSP00000387277.1:p.Gln57=
ENST00000421804.6:c.697_699delinsCAA	ENSP00000389152.2:p.Gln233=
ENST00000439966.5:c.*170_*172delinsCAA	ENSP00000402129.1:n.*170_*172delinsCAA
ENST00000616902.4:c.-519_-517delinsCAA	ENSP00000482824.1:n.-519_-517delinsCAA
NM_006343.2:c.697_699delinsCAA	NP_006334.2:p.Gln233=
XM_005263565.3:c.697_699delinsCAA	XP_005263622.1:p.Gln233=
XM_005263568.3:c.697_699delinsCAA	XP_005263625.1:p.Gln233=
XM_011510490.1:c.508_510delinsCAA	XP_011508792.1:p.Gln170=
XM_005263565.4:c.697_699delinsCAA	XP_005263622.1:p.Gln233=
XM_005263568.4:c.697_699delinsCAA	XP_005263625.1:p.Gln233=
XM_011510490.3:c.508_510delinsCAA	XP_011508792.1:p.Gln170=
XM_017003164.1:c.508_510delinsCAA	XP_016858653.1:p.Gln170=
XM_017003165.2:c.-571_-569delinsCAA	XP_016858654.1:n.-571_-569delinsCAA
NM_006343.3:c.697_699delinsCAA MANE Select	NP_006334.2:p.Gln233=