Canonical Allele Identifier: CA2751717384

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947712_111947713insACA , CM000664.2:g.111947712_111947713insACA	GRCh38
NC_000002.11:g.112705289_112705290insACA , CM000664.1:g.112705289_112705290insACA	GRCh37
NC_000002.10:g.112421760_112421761insACA	NCBI36
NG_011607.1:g.54099_54100insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+145_757+146insACA MANE Select	ENSP00000295408.4:n.757+145_757+146insACA
ENST00000295408.8:c.757+145_757+146insACA	ENSP00000295408.4:n.757+145_757+146insACA
ENST00000409780.5:c.229+145_229+146insACA	ENSP00000387277.1:n.229+145_229+146insACA
ENST00000421804.6:c.757+145_757+146insACA	ENSP00000389152.2:n.757+145_757+146insACA
ENST00000439966.5:c.*230+145_*230+146insACA	ENSP00000402129.1:n.*230+145_*230+146insACA
ENST00000616902.4:c.-459+145_-459+146insACA	ENSP00000482824.1:n.-459+145_-459+146insACA
NM_006343.2:c.757+145_757+146insACA	NP_006334.2:n.757+145_757+146insACA
XM_005263565.3:c.757+145_757+146insACA	XP_005263622.1:n.757+145_757+146insACA
XM_005263568.3:c.757+145_757+146insACA	XP_005263625.1:n.757+145_757+146insACA
XM_011510490.1:c.568+145_568+146insACA	XP_011508792.1:n.568+145_568+146insACA
XM_005263565.4:c.757+145_757+146insACA	XP_005263622.1:n.757+145_757+146insACA
XM_005263568.4:c.757+145_757+146insACA	XP_005263625.1:n.757+145_757+146insACA
XM_011510490.3:c.568+145_568+146insACA	XP_011508792.1:n.568+145_568+146insACA
XM_017003164.1:c.568+145_568+146insACA	XP_016858653.1:n.568+145_568+146insACA
XM_017003165.2:c.-511+145_-511+146insACA	XP_016858654.1:n.-511+145_-511+146insACA
NM_006343.3:c.757+145_757+146insACA MANE Select	NP_006334.2:n.757+145_757+146insACA