Canonical Allele Identifier: CA1279566595

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997480_111997487delinsAGTCTCCC , CM000664.2:g.111997480_111997487delinsAGTCTCCC	GRCh38
NC_000002.11:g.112755057_112755064delinsAGTCTCCC , CM000664.1:g.112755057_112755064delinsAGTCTCCC	GRCh37
NC_000002.10:g.112471528_112471535delinsAGTCTCCC	NCBI36
NG_011607.1:g.103867_103874delinsAGTCTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1604+4_1604+11delinsAGTCTCCC MANE Select	ENSP00000295408.4:n.1604+4_1604+11delinsAGTCTCCC
ENST00000295408.8:c.1604+4_1604+11delinsAGTCTCCC	ENSP00000295408.4:n.1604+4_1604+11delinsAGTCTCCC
ENST00000409780.5:c.1076+4_1076+11delinsAGTCTCCC	ENSP00000387277.1:n.1076+4_1076+11delinsAGTCTCCC
ENST00000421804.6:c.1604+4_1604+11delinsAGTCTCCC	ENSP00000389152.2:n.1604+4_1604+11delinsAGTCTCCC
ENST00000439966.5:c.*1077+4_*1077+11delinsAGTCTCCC	ENSP00000402129.1:n.*1077+4_*1077+11delinsAGTCTCCC
ENST00000473065.1:n.107+4_107+11delinsAGTCTCCC
ENST00000616902.4:c.569+4_569+11delinsAGTCTCCC	ENSP00000482824.1:n.569+4_569+11delinsAGTCTCCC
NM_006343.2:c.1604+4_1604+11delinsAGTCTCCC	NP_006334.2:n.1604+4_1604+11delinsAGTCTCCC
XM_005263565.3:c.1604+4_1604+11delinsAGTCTCCC	XP_005263622.1:n.1604+4_1604+11delinsAGTCTCCC
XM_005263568.3:c.1604+4_1604+11delinsAGTCTCCC	XP_005263625.1:n.1604+4_1604+11delinsAGTCTCCC
XM_011510490.1:c.1415+4_1415+11delinsAGTCTCCC	XP_011508792.1:n.1415+4_1415+11delinsAGTCTCCC
XM_011510491.1:c.389+4_389+11delinsAGTCTCCC	XP_011508793.1:n.389+4_389+11delinsAGTCTCCC
XM_005263565.4:c.1604+4_1604+11delinsAGTCTCCC	XP_005263622.1:n.1604+4_1604+11delinsAGTCTCCC
XM_005263568.4:c.1604+4_1604+11delinsAGTCTCCC	XP_005263625.1:n.1604+4_1604+11delinsAGTCTCCC
XM_011510490.3:c.1415+4_1415+11delinsAGTCTCCC	XP_011508792.1:n.1415+4_1415+11delinsAGTCTCCC
XM_017003164.1:c.1415+4_1415+11delinsAGTCTCCC	XP_016858653.1:n.1415+4_1415+11delinsAGTCTCCC
XM_017003165.2:c.389+4_389+11delinsAGTCTCCC	XP_016858654.1:n.389+4_389+11delinsAGTCTCCC
NM_006343.3:c.1604+4_1604+11delinsAGTCTCCC MANE Select	NP_006334.2:n.1604+4_1604+11delinsAGTCTCCC