Canonical Allele Identifier: CA1279536500

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111929415_111929418delinsACCT , CM000664.2:g.111929415_111929418delinsACCT	GRCh38
NC_000002.11:g.112686992_112686995delinsACCT , CM000664.1:g.112686992_112686995delinsACCT	GRCh37
NC_000002.10:g.112403463_112403466delinsACCT	NCBI36
NG_011607.1:g.35802_35805delinsACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.357_360delinsACCT MANE Select	ENSP00000295408.4:p.Val119=
ENST00000295408.8:c.357_360delinsACCT	ENSP00000295408.4:p.Val119=
ENST00000409780.5:c.-46-15545_-46-15542delinsACCT	ENSP00000387277.1:n.-46-15545_-46-15542delinsACCT
ENST00000421804.6:c.357_360delinsACCT	ENSP00000389152.2:p.Val119=
ENST00000439966.5:c.246+111_246+114delinsACCT	ENSP00000402129.1:n.246+111_246+114delinsACCT
ENST00000616902.4:c.-859_-856delinsACCT	ENSP00000482824.1:n.-859_-856delinsACCT
NM_006343.2:c.357_360delinsACCT	NP_006334.2:p.Val119=
XM_005263565.3:c.357_360delinsACCT	XP_005263622.1:p.Val119=
XM_005263568.3:c.357_360delinsACCT	XP_005263625.1:p.Val119=
XM_011510490.1:c.168_171delinsACCT	XP_011508792.1:p.Val56=
XM_005263565.4:c.357_360delinsACCT	XP_005263622.1:p.Val119=
XM_005263568.4:c.357_360delinsACCT	XP_005263625.1:p.Val119=
XM_011510490.3:c.168_171delinsACCT	XP_011508792.1:p.Val56=
XM_017003164.1:c.168_171delinsACCT	XP_016858653.1:p.Val56=
XM_017003165.2:c.-911_-908delinsACCT	XP_016858654.1:n.-911_-908delinsACCT
NM_006343.3:c.357_360delinsACCT MANE Select	NP_006334.2:p.Val119=