Canonical Allele Identifier: CA2523887056

Gene: MERTK

Linked Data

• ClinVar Variation Id: 1582895
• ClinVar RCV Id: RCV002097610
• dbSNP Id: rs2104411607

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112008367C>A , CM000664.2:g.112008367C>A	GRCh38
NC_000002.11:g.112765944C>A , CM000664.1:g.112765944C>A	GRCh37
NC_000002.10:g.112482415C>A	NCBI36
NG_011607.1:g.114754C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295408.9:c.1868-16C>A MANE Select	ENSP00000295408.4:n.1868-16C>A
ENST00000295408.8:c.1868-16C>A	ENSP00000295408.4:n.1868-16C>A
ENST00000409780.5:c.1340-16C>A	ENSP00000387277.1:n.1340-16C>A
ENST00000421804.6:c.1868-16C>A	ENSP00000389152.2:n.1868-16C>A
ENST00000439966.5:c.*1341-16C>A	ENSP00000402129.1:n.*1341-16C>A
ENST00000616902.4:c.833-16C>A	ENSP00000482824.1:n.833-16C>A
NM_006343.2:c.1868-16C>A	NP_006334.2:n.1868-16C>A
XM_005263565.3:c.1868-16C>A	XP_005263622.1:n.1868-16C>A
XM_005263568.3:c.1868-16C>A	XP_005263625.1:n.1868-16C>A
XM_011510490.1:c.1679-16C>A	XP_011508792.1:n.1679-16C>A
XM_011510491.1:c.653-16C>A	XP_011508793.1:n.653-16C>A
XM_005263565.4:c.1868-16C>A	XP_005263622.1:n.1868-16C>A
XM_005263568.4:c.1868-16C>A	XP_005263625.1:n.1868-16C>A
XM_011510490.3:c.1679-16C>A	XP_011508792.1:n.1679-16C>A
XM_017003164.1:c.1679-16C>A	XP_016858653.1:n.1679-16C>A
XM_017003165.2:c.653-16C>A	XP_016858654.1:n.653-16C>A
NM_006343.3:c.1868-16C>A MANE Select	NP_006334.2:n.1868-16C>A