Canonical Allele Identifier: CA348226751

Gene: MERTK

Linked Data

• gnomAD v4: 2-111929483-A-G
• MyVariant Identifiers: chr2:g.112687060A>G (hg19) ; chr2:g.111929483A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111929483A>G , CM000664.2:g.111929483A>G	GRCh38
NC_000002.11:g.112687060A>G , CM000664.1:g.112687060A>G	GRCh37
NC_000002.10:g.112403531A>G	NCBI36
NG_011607.1:g.35870A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.425A>G MANE Select	ENSP00000295408.4:p.His142Arg
ENST00000295408.8:c.425A>G	ENSP00000295408.4:p.His142Arg
ENST00000409780.5:c.-46-15477A>G	ENSP00000387277.1:n.-46-15477A>G
ENST00000421804.6:c.425A>G	ENSP00000389152.2:p.His142Arg
ENST00000439966.5:c.246+179A>G	ENSP00000402129.1:n.246+179A>G
ENST00000616902.4:c.-791A>G	ENSP00000482824.1:n.-791A>G
NM_006343.2:c.425A>G	NP_006334.2:p.His142Arg
XM_005263565.3:c.425A>G	XP_005263622.1:p.His142Arg
XM_005263568.3:c.425A>G	XP_005263625.1:p.His142Arg
XM_011510490.1:c.236A>G	XP_011508792.1:p.His79Arg
XM_005263565.4:c.425A>G	XP_005263622.1:p.His142Arg
XM_005263568.4:c.425A>G	XP_005263625.1:p.His142Arg
XM_011510490.3:c.236A>G	XP_011508792.1:p.His79Arg
XM_017003164.1:c.236A>G	XP_016858653.1:p.His79Arg
XM_017003165.2:c.-843A>G	XP_016858654.1:n.-843A>G
NM_006343.3:c.425A>G MANE Select	NP_006334.2:p.His142Arg