Canonical Allele Identifier: CA1279544294

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947410_111947411delinsTA , CM000664.2:g.111947410_111947411delinsTA	GRCh38
NC_000002.11:g.112704987_112704988delinsTA , CM000664.1:g.112704987_112704988delinsTA	GRCh37
NC_000002.10:g.112421458_112421459delinsTA	NCBI36
NG_011607.1:g.53797_53798delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.600_601delinsTA MANE Select	ENSP00000295408.4:p.Thr200=
ENST00000295408.8:c.600_601delinsTA	ENSP00000295408.4:p.Thr200=
ENST00000409780.5:c.72_73delinsTA	ENSP00000387277.1:p.Thr24=
ENST00000421804.6:c.600_601delinsTA	ENSP00000389152.2:p.Thr200=
ENST00000439966.5:c.*73_*74delinsTA	ENSP00000402129.1:n.*73_*74delinsTA
ENST00000616902.4:c.-616_-615delinsTA	ENSP00000482824.1:n.-616_-615delinsTA
NM_006343.2:c.600_601delinsTA	NP_006334.2:p.Thr200=
XM_005263565.3:c.600_601delinsTA	XP_005263622.1:p.Thr200=
XM_005263568.3:c.600_601delinsTA	XP_005263625.1:p.Thr200=
XM_011510490.1:c.411_412delinsTA	XP_011508792.1:p.Thr137=
XM_005263565.4:c.600_601delinsTA	XP_005263622.1:p.Thr200=
XM_005263568.4:c.600_601delinsTA	XP_005263625.1:p.Thr200=
XM_011510490.3:c.411_412delinsTA	XP_011508792.1:p.Thr137=
XM_017003164.1:c.411_412delinsTA	XP_016858653.1:p.Thr137=
XM_017003165.2:c.-668_-667delinsTA	XP_016858654.1:n.-668_-667delinsTA
NM_006343.3:c.600_601delinsTA MANE Select	NP_006334.2:p.Thr200=