Canonical Allele Identifier: CA2751719951

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112008581_112008582insACT , CM000664.2:g.112008581_112008582insACT	GRCh38
NC_000002.11:g.112766158_112766159insACT , CM000664.1:g.112766158_112766159insACT	GRCh37
NC_000002.10:g.112482629_112482630insACT	NCBI36
NG_011607.1:g.114968_114969insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1960+106_1960+107insACT MANE Select	ENSP00000295408.4:n.1960+106_1960+107insACT
ENST00000295408.8:c.1960+106_1960+107insACT	ENSP00000295408.4:n.1960+106_1960+107insACT
ENST00000409780.5:c.1432+106_1432+107insACT	ENSP00000387277.1:n.1432+106_1432+107insACT
ENST00000421804.6:c.1960+106_1960+107insACT	ENSP00000389152.2:n.1960+106_1960+107insACT
ENST00000439966.5:c.*1433+106_*1433+107insACT	ENSP00000402129.1:n.*1433+106_*1433+107insACT
ENST00000616902.4:c.925+106_925+107insACT	ENSP00000482824.1:n.925+106_925+107insACT
NM_006343.2:c.1960+106_1960+107insACT	NP_006334.2:n.1960+106_1960+107insACT
XM_005263565.3:c.1960+106_1960+107insACT	XP_005263622.1:n.1960+106_1960+107insACT
XM_005263568.3:c.1960+106_1960+107insACT	XP_005263625.1:n.1960+106_1960+107insACT
XM_011510490.1:c.1771+106_1771+107insACT	XP_011508792.1:n.1771+106_1771+107insACT
XM_011510491.1:c.745+106_745+107insACT	XP_011508793.1:n.745+106_745+107insACT
XM_005263565.4:c.1960+106_1960+107insACT	XP_005263622.1:n.1960+106_1960+107insACT
XM_005263568.4:c.1960+106_1960+107insACT	XP_005263625.1:n.1960+106_1960+107insACT
XM_011510490.3:c.1771+106_1771+107insACT	XP_011508792.1:n.1771+106_1771+107insACT
XM_017003164.1:c.1771+106_1771+107insACT	XP_016858653.1:n.1771+106_1771+107insACT
XM_017003165.2:c.745+106_745+107insACT	XP_016858654.1:n.745+106_745+107insACT
NM_006343.3:c.1960+106_1960+107insACT MANE Select	NP_006334.2:n.1960+106_1960+107insACT