Canonical Allele Identifier: CA2577070619

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112008553_112008555del , CM000664.2:g.112008553_112008555del	GRCh38
NC_000002.11:g.112766130_112766132del , CM000664.1:g.112766130_112766132del	GRCh37
NC_000002.10:g.112482601_112482603del	NCBI36
NG_011607.1:g.114940_114942del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1960+78_1960+80del MANE Select	ENSP00000295408.4:n.1960+78_1960+80del
ENST00000295408.8:c.1960+78_1960+80del	ENSP00000295408.4:n.1960+78_1960+80del
ENST00000409780.5:c.1432+78_1432+80del	ENSP00000387277.1:n.1432+78_1432+80del
ENST00000421804.6:c.1960+78_1960+80del	ENSP00000389152.2:n.1960+78_1960+80del
ENST00000439966.5:c.*1433+78_*1433+80del	ENSP00000402129.1:n.*1433+78_*1433+80del
ENST00000616902.4:c.925+78_925+80del	ENSP00000482824.1:n.925+78_925+80del
NM_006343.2:c.1960+78_1960+80del	NP_006334.2:n.1960+78_1960+80del
XM_005263565.3:c.1960+78_1960+80del	XP_005263622.1:n.1960+78_1960+80del
XM_005263568.3:c.1960+78_1960+80del	XP_005263625.1:n.1960+78_1960+80del
XM_011510490.1:c.1771+78_1771+80del	XP_011508792.1:n.1771+78_1771+80del
XM_011510491.1:c.745+78_745+80del	XP_011508793.1:n.745+78_745+80del
XM_005263565.4:c.1960+78_1960+80del	XP_005263622.1:n.1960+78_1960+80del
XM_005263568.4:c.1960+78_1960+80del	XP_005263625.1:n.1960+78_1960+80del
XM_011510490.3:c.1771+78_1771+80del	XP_011508792.1:n.1771+78_1771+80del
XM_017003164.1:c.1771+78_1771+80del	XP_016858653.1:n.1771+78_1771+80del
XM_017003165.2:c.745+78_745+80del	XP_016858654.1:n.745+78_745+80del
NM_006343.3:c.1960+78_1960+80del MANE Select	NP_006334.2:n.1960+78_1960+80del