Canonical Allele Identifier: CA2751719969

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112008604_112008609del , CM000664.2:g.112008604_112008609del	GRCh38
NC_000002.11:g.112766181_112766186del , CM000664.1:g.112766181_112766186del	GRCh37
NC_000002.10:g.112482652_112482657del	NCBI36
NG_011607.1:g.114991_114996del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1960+129_1960+134del MANE Select	ENSP00000295408.4:n.1960+129_1960+134del
ENST00000295408.8:c.1960+129_1960+134del	ENSP00000295408.4:n.1960+129_1960+134del
ENST00000409780.5:c.1432+129_1432+134del	ENSP00000387277.1:n.1432+129_1432+134del
ENST00000421804.6:c.1960+129_1960+134del	ENSP00000389152.2:n.1960+129_1960+134del
ENST00000439966.5:c.*1433+129_*1433+134del	ENSP00000402129.1:n.*1433+129_*1433+134del
ENST00000616902.4:c.925+129_925+134del	ENSP00000482824.1:n.925+129_925+134del
NM_006343.2:c.1960+129_1960+134del	NP_006334.2:n.1960+129_1960+134del
XM_005263565.3:c.1960+129_1960+134del	XP_005263622.1:n.1960+129_1960+134del
XM_005263568.3:c.1960+129_1960+134del	XP_005263625.1:n.1960+129_1960+134del
XM_011510490.1:c.1771+129_1771+134del	XP_011508792.1:n.1771+129_1771+134del
XM_011510491.1:c.745+129_745+134del	XP_011508793.1:n.745+129_745+134del
XM_005263565.4:c.1960+129_1960+134del	XP_005263622.1:n.1960+129_1960+134del
XM_005263568.4:c.1960+129_1960+134del	XP_005263625.1:n.1960+129_1960+134del
XM_011510490.3:c.1771+129_1771+134del	XP_011508792.1:n.1771+129_1771+134del
XM_017003164.1:c.1771+129_1771+134del	XP_016858653.1:n.1771+129_1771+134del
XM_017003165.2:c.745+129_745+134del	XP_016858654.1:n.745+129_745+134del
NM_006343.3:c.1960+129_1960+134del MANE Select	NP_006334.2:n.1960+129_1960+134del