Canonical Allele Identifier: CA348226882

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112687093T>G (hg19) ; chr2:g.111929516T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111929516T>G , CM000664.2:g.111929516T>G	GRCh38
NC_000002.11:g.112687093T>G , CM000664.1:g.112687093T>G	GRCh37
NC_000002.10:g.112403564T>G	NCBI36
NG_011607.1:g.35903T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.458T>G MANE Select	ENSP00000295408.4:p.Val153Gly
ENST00000295408.8:c.458T>G	ENSP00000295408.4:p.Val153Gly
ENST00000409780.5:c.-46-15444T>G	ENSP00000387277.1:n.-46-15444T>G
ENST00000421804.6:c.458T>G	ENSP00000389152.2:p.Val153Gly
ENST00000439966.5:c.246+212T>G	ENSP00000402129.1:n.246+212T>G
ENST00000616902.4:c.-758T>G	ENSP00000482824.1:n.-758T>G
NM_006343.2:c.458T>G	NP_006334.2:p.Val153Gly
XM_005263565.3:c.458T>G	XP_005263622.1:p.Val153Gly
XM_005263568.3:c.458T>G	XP_005263625.1:p.Val153Gly
XM_011510490.1:c.269T>G	XP_011508792.1:p.Val90Gly
XM_005263565.4:c.458T>G	XP_005263622.1:p.Val153Gly
XM_005263568.4:c.458T>G	XP_005263625.1:p.Val153Gly
XM_011510490.3:c.269T>G	XP_011508792.1:p.Val90Gly
XM_017003164.1:c.269T>G	XP_016858653.1:p.Val90Gly
XM_017003165.2:c.-810T>G	XP_016858654.1:n.-810T>G
NM_006343.3:c.458T>G MANE Select	NP_006334.2:p.Val153Gly