Canonical Allele Identifier: CA2751717294

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947606del , CM000664.2:g.111947606del	GRCh38
NC_000002.11:g.112705183del , CM000664.1:g.112705183del	GRCh37
NC_000002.10:g.112421654del	NCBI36
NG_011607.1:g.53993del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+39del MANE Select	ENSP00000295408.4:n.757+39del
ENST00000295408.8:c.757+39del	ENSP00000295408.4:n.757+39del
ENST00000409780.5:c.229+39del	ENSP00000387277.1:n.229+39del
ENST00000421804.6:c.757+39del	ENSP00000389152.2:n.757+39del
ENST00000439966.5:c.*230+39del	ENSP00000402129.1:n.*230+39del
ENST00000616902.4:c.-459+39del	ENSP00000482824.1:n.-459+39del
NM_006343.2:c.757+39del	NP_006334.2:n.757+39del
XM_005263565.3:c.757+39del	XP_005263622.1:n.757+39del
XM_005263568.3:c.757+39del	XP_005263625.1:n.757+39del
XM_011510490.1:c.568+39del	XP_011508792.1:n.568+39del
XM_005263565.4:c.757+39del	XP_005263622.1:n.757+39del
XM_005263568.4:c.757+39del	XP_005263625.1:n.757+39del
XM_011510490.3:c.568+39del	XP_011508792.1:n.568+39del
XM_017003164.1:c.568+39del	XP_016858653.1:n.568+39del
XM_017003165.2:c.-511+39del	XP_016858654.1:n.-511+39del
NM_006343.3:c.757+39del MANE Select	NP_006334.2:n.757+39del