Canonical Allele Identifier: CA2751719932

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112008561_112008562del , CM000664.2:g.112008561_112008562del	GRCh38
NC_000002.11:g.112766138_112766139del , CM000664.1:g.112766138_112766139del	GRCh37
NC_000002.10:g.112482609_112482610del	NCBI36
NG_011607.1:g.114948_114949del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1960+86_1960+87del MANE Select	ENSP00000295408.4:n.1960+86_1960+87del
ENST00000295408.8:c.1960+86_1960+87del	ENSP00000295408.4:n.1960+86_1960+87del
ENST00000409780.5:c.1432+86_1432+87del	ENSP00000387277.1:n.1432+86_1432+87del
ENST00000421804.6:c.1960+86_1960+87del	ENSP00000389152.2:n.1960+86_1960+87del
ENST00000439966.5:c.*1433+86_*1433+87del	ENSP00000402129.1:n.*1433+86_*1433+87del
ENST00000616902.4:c.925+86_925+87del	ENSP00000482824.1:n.925+86_925+87del
NM_006343.2:c.1960+86_1960+87del	NP_006334.2:n.1960+86_1960+87del
XM_005263565.3:c.1960+86_1960+87del	XP_005263622.1:n.1960+86_1960+87del
XM_005263568.3:c.1960+86_1960+87del	XP_005263625.1:n.1960+86_1960+87del
XM_011510490.1:c.1771+86_1771+87del	XP_011508792.1:n.1771+86_1771+87del
XM_011510491.1:c.745+86_745+87del	XP_011508793.1:n.745+86_745+87del
XM_005263565.4:c.1960+86_1960+87del	XP_005263622.1:n.1960+86_1960+87del
XM_005263568.4:c.1960+86_1960+87del	XP_005263625.1:n.1960+86_1960+87del
XM_011510490.3:c.1771+86_1771+87del	XP_011508792.1:n.1771+86_1771+87del
XM_017003164.1:c.1771+86_1771+87del	XP_016858653.1:n.1771+86_1771+87del
XM_017003165.2:c.745+86_745+87del	XP_016858654.1:n.745+86_745+87del
NM_006343.3:c.1960+86_1960+87del MANE Select	NP_006334.2:n.1960+86_1960+87del