Canonical Allele Identifier: CA348231242

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112754950C>A (hg19) ; chr2:g.111997373C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997373C>A , CM000664.2:g.111997373C>A	GRCh38
NC_000002.11:g.112754950C>A , CM000664.1:g.112754950C>A	GRCh37
NC_000002.10:g.112471421C>A	NCBI36
NG_011607.1:g.103760C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1501C>A MANE Select	ENSP00000295408.4:p.Pro501Thr
ENST00000295408.8:c.1501C>A	ENSP00000295408.4:p.Pro501Thr
ENST00000409780.5:c.973C>A	ENSP00000387277.1:p.Pro325Thr
ENST00000421804.6:c.1501C>A	ENSP00000389152.2:p.Pro501Thr
ENST00000439966.5:c.*974C>A	ENSP00000402129.1:n.*974C>A
ENST00000473065.1:n.4C>A
ENST00000616902.4:c.470C>A	ENSP00000482824.1:p.Ser157Tyr
NM_006343.2:c.1501C>A	NP_006334.2:p.Pro501Thr
XM_005263565.3:c.1501C>A	XP_005263622.1:p.Pro501Thr
XM_005263568.3:c.1501C>A	XP_005263625.1:p.Pro501Thr
XM_011510490.1:c.1312C>A	XP_011508792.1:p.Pro438Thr
XM_011510491.1:c.286C>A	XP_011508793.1:p.Pro96Thr
XM_005263565.4:c.1501C>A	XP_005263622.1:p.Pro501Thr
XM_005263568.4:c.1501C>A	XP_005263625.1:p.Pro501Thr
XM_011510490.3:c.1312C>A	XP_011508792.1:p.Pro438Thr
XM_017003164.1:c.1312C>A	XP_016858653.1:p.Pro438Thr
XM_017003165.2:c.286C>A	XP_016858654.1:p.Pro96Thr
NM_006343.3:c.1501C>A MANE Select	NP_006334.2:p.Pro501Thr