Canonical Allele Identifier: CA348231244

Gene: MERTK

Linked Data

• gnomAD v4: 2-111997373-C-G
• MyVariant Identifiers: chr2:g.112754950C>G (hg19) ; chr2:g.111997373C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1501C>G MANE Select	ENSP00000295408.4:p.Pro501Ala
ENST00000295408.8:c.1501C>G	ENSP00000295408.4:p.Pro501Ala
ENST00000409780.5:c.973C>G	ENSP00000387277.1:p.Pro325Ala
ENST00000421804.6:c.1501C>G	ENSP00000389152.2:p.Pro501Ala
ENST00000439966.5:c.*974C>G	ENSP00000402129.1:n.*974C>G
ENST00000473065.1:n.4C>G
ENST00000616902.4:c.470C>G	ENSP00000482824.1:p.Ser157Cys
NM_006343.2:c.1501C>G	NP_006334.2:p.Pro501Ala
XM_005263565.3:c.1501C>G	XP_005263622.1:p.Pro501Ala
XM_005263568.3:c.1501C>G	XP_005263625.1:p.Pro501Ala
XM_011510490.1:c.1312C>G	XP_011508792.1:p.Pro438Ala
XM_011510491.1:c.286C>G	XP_011508793.1:p.Pro96Ala
XM_005263565.4:c.1501C>G	XP_005263622.1:p.Pro501Ala
XM_005263568.4:c.1501C>G	XP_005263625.1:p.Pro501Ala
XM_011510490.3:c.1312C>G	XP_011508792.1:p.Pro438Ala
XM_017003164.1:c.1312C>G	XP_016858653.1:p.Pro438Ala
XM_017003165.2:c.286C>G	XP_016858654.1:p.Pro96Ala
NM_006343.3:c.1501C>G MANE Select	NP_006334.2:p.Pro501Ala