Canonical Allele Identifier: CA2577070492

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997334del , CM000664.2:g.111997334del	GRCh38
NC_000002.11:g.112754911del , CM000664.1:g.112754911del	GRCh37
NC_000002.10:g.112471382del	NCBI36
NG_011607.1:g.103721del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1462del MANE Select	ENSP00000295408.4:p.Tyr488MetfsTer27
ENST00000295408.8:c.1462del	ENSP00000295408.4:p.Tyr488MetfsTer27
ENST00000409780.5:c.934del	ENSP00000387277.1:p.Tyr312MetfsTer27
ENST00000421804.6:c.1462del	ENSP00000389152.2:p.Tyr488MetfsTer27
ENST00000439966.5:c.*935del	ENSP00000402129.1:n.*935del
ENST00000616902.4:c.431del	ENSP00000482824.1:p.Leu144TyrfsTer26
NM_006343.2:c.1462del	NP_006334.2:p.Tyr488MetfsTer27
XM_005263565.3:c.1462del	XP_005263622.1:p.Tyr488MetfsTer27
XM_005263568.3:c.1462del	XP_005263625.1:p.Tyr488MetfsTer27
XM_011510490.1:c.1273del	XP_011508792.1:p.Tyr425MetfsTer27
XM_011510491.1:c.247del	XP_011508793.1:p.Tyr83MetfsTer27
XM_005263565.4:c.1462del	XP_005263622.1:p.Tyr488MetfsTer27
XM_005263568.4:c.1462del	XP_005263625.1:p.Tyr488MetfsTer27
XM_011510490.3:c.1273del	XP_011508792.1:p.Tyr425MetfsTer27
XM_017003164.1:c.1273del	XP_016858653.1:p.Tyr425MetfsTer27
XM_017003165.2:c.247del	XP_016858654.1:p.Tyr83MetfsTer27
NM_006343.3:c.1462del MANE Select	NP_006334.2:p.Tyr488MetfsTer27