Canonical Allele Identifier: CA348232412

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111968253G>A , CM000664.2:g.111968253G>A	GRCh38
NC_000002.11:g.112725830G>A , CM000664.1:g.112725830G>A	GRCh37
NC_000002.10:g.112442301G>A	NCBI36
NG_011607.1:g.74640G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006343.3:c.960+1G>A MANE Select	NP_006334.2:n.960+1G>A
ENST00000295408.9:c.960+1G>A MANE Select	ENSP00000295408.4:n.960+1G>A
NM_006343.2:c.960+1G>A	NP_006334.2:n.960+1G>A
ENST00000295408.8:c.960+1G>A	ENSP00000295408.4:n.960+1G>A
ENST00000409780.5:c.432+1G>A	ENSP00000387277.1:n.432+1G>A
ENST00000421804.6:c.960+1G>A	ENSP00000389152.2:n.960+1G>A
ENST00000439966.5:c.*433+1G>A	ENSP00000402129.1:n.*433+1G>A
ENST00000616902.4:c.-256+1G>A	ENSP00000482824.1:n.-256+1G>A
XM_005263565.3:c.960+1G>A	XP_005263622.1:n.960+1G>A
XM_005263565.4:c.960+1G>A	XP_005263622.1:n.960+1G>A
XM_005263568.3:c.960+1G>A	XP_005263625.1:n.960+1G>A
XM_005263568.4:c.960+1G>A	XP_005263625.1:n.960+1G>A
XM_011510490.1:c.771+1G>A	XP_011508792.1:n.771+1G>A
XM_011510490.3:c.771+1G>A	XP_011508792.1:n.771+1G>A
XM_017003164.1:c.771+1G>A	XP_016858653.1:n.771+1G>A
XM_017003165.2:c.-308+1G>A	XP_016858654.1:n.-308+1G>A