Canonical Allele Identifier: CA2751717297

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947607_111947608insTCA , CM000664.2:g.111947607_111947608insTCA	GRCh38
NC_000002.11:g.112705184_112705185insTCA , CM000664.1:g.112705184_112705185insTCA	GRCh37
NC_000002.10:g.112421655_112421656insTCA	NCBI36
NG_011607.1:g.53994_53995insTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+40_757+41insTCA MANE Select	ENSP00000295408.4:n.757+40_757+41insTCA
ENST00000295408.8:c.757+40_757+41insTCA	ENSP00000295408.4:n.757+40_757+41insTCA
ENST00000409780.5:c.229+40_229+41insTCA	ENSP00000387277.1:n.229+40_229+41insTCA
ENST00000421804.6:c.757+40_757+41insTCA	ENSP00000389152.2:n.757+40_757+41insTCA
ENST00000439966.5:c.*230+40_*230+41insTCA	ENSP00000402129.1:n.*230+40_*230+41insTCA
ENST00000616902.4:c.-459+40_-459+41insTCA	ENSP00000482824.1:n.-459+40_-459+41insTCA
NM_006343.2:c.757+40_757+41insTCA	NP_006334.2:n.757+40_757+41insTCA
XM_005263565.3:c.757+40_757+41insTCA	XP_005263622.1:n.757+40_757+41insTCA
XM_005263568.3:c.757+40_757+41insTCA	XP_005263625.1:n.757+40_757+41insTCA
XM_011510490.1:c.568+40_568+41insTCA	XP_011508792.1:n.568+40_568+41insTCA
XM_005263565.4:c.757+40_757+41insTCA	XP_005263622.1:n.757+40_757+41insTCA
XM_005263568.4:c.757+40_757+41insTCA	XP_005263625.1:n.757+40_757+41insTCA
XM_011510490.3:c.568+40_568+41insTCA	XP_011508792.1:n.568+40_568+41insTCA
XM_017003164.1:c.568+40_568+41insTCA	XP_016858653.1:n.568+40_568+41insTCA
XM_017003165.2:c.-511+40_-511+41insTCA	XP_016858654.1:n.-511+40_-511+41insTCA
NM_006343.3:c.757+40_757+41insTCA MANE Select	NP_006334.2:n.757+40_757+41insTCA