Canonical Allele Identifier: CA2751717373
Gene: MERTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111947683_111947684insAGTA , CM000664.2:g.111947683_111947684insAGTA GRCh38
NC_000002.11:g.112705260_112705261insAGTA , CM000664.1:g.112705260_112705261insAGTA GRCh37
NC_000002.10:g.112421731_112421732insAGTA NCBI36
NG_011607.1:g.54070_54071insAGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295408.9:c.757+116_757+117insAGTA MANE Select ENSP00000295408.4:n.757+116_757+117insAGTA
ENST00000295408.8:c.757+116_757+117insAGTA ENSP00000295408.4:n.757+116_757+117insAGTA
ENST00000409780.5:c.229+116_229+117insAGTA ENSP00000387277.1:n.229+116_229+117insAGTA
ENST00000421804.6:c.757+116_757+117insAGTA ENSP00000389152.2:n.757+116_757+117insAGTA
ENST00000439966.5:c.*230+116_*230+117insAGTA ENSP00000402129.1:n.*230+116_*230+117insAGTA
ENST00000616902.4:c.-459+116_-459+117insAGTA ENSP00000482824.1:n.-459+116_-459+117insAGTA
NM_006343.2:c.757+116_757+117insAGTA NP_006334.2:n.757+116_757+117insAGTA
XM_005263565.3:c.757+116_757+117insAGTA XP_005263622.1:n.757+116_757+117insAGTA
XM_005263568.3:c.757+116_757+117insAGTA XP_005263625.1:n.757+116_757+117insAGTA
XM_011510490.1:c.568+116_568+117insAGTA XP_011508792.1:n.568+116_568+117insAGTA
XM_005263565.4:c.757+116_757+117insAGTA XP_005263622.1:n.757+116_757+117insAGTA
XM_005263568.4:c.757+116_757+117insAGTA XP_005263625.1:n.757+116_757+117insAGTA
XM_011510490.3:c.568+116_568+117insAGTA XP_011508792.1:n.568+116_568+117insAGTA
XM_017003164.1:c.568+116_568+117insAGTA XP_016858653.1:n.568+116_568+117insAGTA
XM_017003165.2:c.-511+116_-511+117insAGTA XP_016858654.1:n.-511+116_-511+117insAGTA
NM_006343.3:c.757+116_757+117insAGTA MANE Select NP_006334.2:n.757+116_757+117insAGTA