Canonical Allele Identifier: CA2577070435

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947494del , CM000664.2:g.111947494del	GRCh38
NC_000002.11:g.112705071del , CM000664.1:g.112705071del	GRCh37
NC_000002.10:g.112421542del	NCBI36
NG_011607.1:g.53881del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.684del MANE Select	ENSP00000295408.4:p.Asn228LysfsTer22
ENST00000295408.8:c.684del	ENSP00000295408.4:p.Asn228LysfsTer22
ENST00000409780.5:c.156del	ENSP00000387277.1:p.Asn52LysfsTer22
ENST00000421804.6:c.684del	ENSP00000389152.2:p.Asn228LysfsTer22
ENST00000439966.5:c.*157del	ENSP00000402129.1:n.*157del
ENST00000616902.4:c.-532del	ENSP00000482824.1:n.-532del
NM_006343.2:c.684del	NP_006334.2:p.Asn228LysfsTer22
XM_005263565.3:c.684del	XP_005263622.1:p.Asn228LysfsTer22
XM_005263568.3:c.684del	XP_005263625.1:p.Asn228LysfsTer22
XM_011510490.1:c.495del	XP_011508792.1:p.Asn165LysfsTer22
XM_005263565.4:c.684del	XP_005263622.1:p.Asn228LysfsTer22
XM_005263568.4:c.684del	XP_005263625.1:p.Asn228LysfsTer22
XM_011510490.3:c.495del	XP_011508792.1:p.Asn165LysfsTer22
XM_017003164.1:c.495del	XP_016858653.1:p.Asn165LysfsTer22
XM_017003165.2:c.-584del	XP_016858654.1:n.-584del
NM_006343.3:c.684del MANE Select	NP_006334.2:p.Asn228LysfsTer22