Canonical Allele Identifier: CA348231296

Gene: MERTK

Linked Data

• gnomAD v4: 2-111997384-C-G
• MyVariant Identifiers: chr2:g.112754961C>G (hg19) ; chr2:g.111997384C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997384C>G , CM000664.2:g.111997384C>G	GRCh38
NC_000002.11:g.112754961C>G , CM000664.1:g.112754961C>G	GRCh37
NC_000002.10:g.112471432C>G	NCBI36
NG_011607.1:g.103771C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1512C>G MANE Select	ENSP00000295408.4:p.Ile504Met
ENST00000295408.8:c.1512C>G	ENSP00000295408.4:p.Ile504Met
ENST00000409780.5:c.984C>G	ENSP00000387277.1:p.Ile328Met
ENST00000421804.6:c.1512C>G	ENSP00000389152.2:p.Ile504Met
ENST00000439966.5:c.*985C>G	ENSP00000402129.1:n.*985C>G
ENST00000473065.1:n.15C>G
ENST00000616902.4:c.481C>G	ENSP00000482824.1:p.His161Asp
NM_006343.2:c.1512C>G	NP_006334.2:p.Ile504Met
XM_005263565.3:c.1512C>G	XP_005263622.1:p.Ile504Met
XM_005263568.3:c.1512C>G	XP_005263625.1:p.Ile504Met
XM_011510490.1:c.1323C>G	XP_011508792.1:p.Ile441Met
XM_011510491.1:c.297C>G	XP_011508793.1:p.Ile99Met
XM_005263565.4:c.1512C>G	XP_005263622.1:p.Ile504Met
XM_005263568.4:c.1512C>G	XP_005263625.1:p.Ile504Met
XM_011510490.3:c.1323C>G	XP_011508792.1:p.Ile441Met
XM_017003164.1:c.1323C>G	XP_016858653.1:p.Ile441Met
XM_017003165.2:c.297C>G	XP_016858654.1:p.Ile99Met
NM_006343.3:c.1512C>G MANE Select	NP_006334.2:p.Ile504Met