Canonical Allele Identifier: CA2751717354

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947662_111947664del , CM000664.2:g.111947662_111947664del	GRCh38
NC_000002.11:g.112705239_112705241del , CM000664.1:g.112705239_112705241del	GRCh37
NC_000002.10:g.112421710_112421712del	NCBI36
NG_011607.1:g.54049_54051del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+95_757+97del MANE Select	ENSP00000295408.4:n.757+95_757+97del
ENST00000295408.8:c.757+95_757+97del	ENSP00000295408.4:n.757+95_757+97del
ENST00000409780.5:c.229+95_229+97del	ENSP00000387277.1:n.229+95_229+97del
ENST00000421804.6:c.757+95_757+97del	ENSP00000389152.2:n.757+95_757+97del
ENST00000439966.5:c.*230+95_*230+97del	ENSP00000402129.1:n.*230+95_*230+97del
ENST00000616902.4:c.-459+95_-459+97del	ENSP00000482824.1:n.-459+95_-459+97del
NM_006343.2:c.757+95_757+97del	NP_006334.2:n.757+95_757+97del
XM_005263565.3:c.757+95_757+97del	XP_005263622.1:n.757+95_757+97del
XM_005263568.3:c.757+95_757+97del	XP_005263625.1:n.757+95_757+97del
XM_011510490.1:c.568+95_568+97del	XP_011508792.1:n.568+95_568+97del
XM_005263565.4:c.757+95_757+97del	XP_005263622.1:n.757+95_757+97del
XM_005263568.4:c.757+95_757+97del	XP_005263625.1:n.757+95_757+97del
XM_011510490.3:c.568+95_568+97del	XP_011508792.1:n.568+95_568+97del
XM_017003164.1:c.568+95_568+97del	XP_016858653.1:n.568+95_568+97del
XM_017003165.2:c.-511+95_-511+97del	XP_016858654.1:n.-511+95_-511+97del
NM_006343.3:c.757+95_757+97del MANE Select	NP_006334.2:n.757+95_757+97del