Canonical Allele Identifier: CA2751719929

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112008554_112008555insAC , CM000664.2:g.112008554_112008555insAC	GRCh38
NC_000002.11:g.112766131_112766132insAC , CM000664.1:g.112766131_112766132insAC	GRCh37
NC_000002.10:g.112482602_112482603insAC	NCBI36
NG_011607.1:g.114941_114942insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1960+79_1960+80insAC MANE Select	ENSP00000295408.4:n.1960+79_1960+80insAC
ENST00000295408.8:c.1960+79_1960+80insAC	ENSP00000295408.4:n.1960+79_1960+80insAC
ENST00000409780.5:c.1432+79_1432+80insAC	ENSP00000387277.1:n.1432+79_1432+80insAC
ENST00000421804.6:c.1960+79_1960+80insAC	ENSP00000389152.2:n.1960+79_1960+80insAC
ENST00000439966.5:c.*1433+79_*1433+80insAC	ENSP00000402129.1:n.*1433+79_*1433+80insAC
ENST00000616902.4:c.925+79_925+80insAC	ENSP00000482824.1:n.925+79_925+80insAC
NM_006343.2:c.1960+79_1960+80insAC	NP_006334.2:n.1960+79_1960+80insAC
XM_005263565.3:c.1960+79_1960+80insAC	XP_005263622.1:n.1960+79_1960+80insAC
XM_005263568.3:c.1960+79_1960+80insAC	XP_005263625.1:n.1960+79_1960+80insAC
XM_011510490.1:c.1771+79_1771+80insAC	XP_011508792.1:n.1771+79_1771+80insAC
XM_011510491.1:c.745+79_745+80insAC	XP_011508793.1:n.745+79_745+80insAC
XM_005263565.4:c.1960+79_1960+80insAC	XP_005263622.1:n.1960+79_1960+80insAC
XM_005263568.4:c.1960+79_1960+80insAC	XP_005263625.1:n.1960+79_1960+80insAC
XM_011510490.3:c.1771+79_1771+80insAC	XP_011508792.1:n.1771+79_1771+80insAC
XM_017003164.1:c.1771+79_1771+80insAC	XP_016858653.1:n.1771+79_1771+80insAC
XM_017003165.2:c.745+79_745+80insAC	XP_016858654.1:n.745+79_745+80insAC
NM_006343.3:c.1960+79_1960+80insAC MANE Select	NP_006334.2:n.1960+79_1960+80insAC