Canonical Allele Identifier: CA348229162

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112705070A>C (hg19) ; chr2:g.111947493A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947493A>C , CM000664.2:g.111947493A>C	GRCh38
NC_000002.11:g.112705070A>C , CM000664.1:g.112705070A>C	GRCh37
NC_000002.10:g.112421541A>C	NCBI36
NG_011607.1:g.53880A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.683A>C MANE Select	ENSP00000295408.4:p.Asn228Thr
ENST00000295408.8:c.683A>C	ENSP00000295408.4:p.Asn228Thr
ENST00000409780.5:c.155A>C	ENSP00000387277.1:p.Asn52Thr
ENST00000421804.6:c.683A>C	ENSP00000389152.2:p.Asn228Thr
ENST00000439966.5:c.*156A>C	ENSP00000402129.1:n.*156A>C
ENST00000616902.4:c.-533A>C	ENSP00000482824.1:n.-533A>C
NM_006343.2:c.683A>C	NP_006334.2:p.Asn228Thr
XM_005263565.3:c.683A>C	XP_005263622.1:p.Asn228Thr
XM_005263568.3:c.683A>C	XP_005263625.1:p.Asn228Thr
XM_011510490.1:c.494A>C	XP_011508792.1:p.Asn165Thr
XM_005263565.4:c.683A>C	XP_005263622.1:p.Asn228Thr
XM_005263568.4:c.683A>C	XP_005263625.1:p.Asn228Thr
XM_011510490.3:c.494A>C	XP_011508792.1:p.Asn165Thr
XM_017003164.1:c.494A>C	XP_016858653.1:p.Asn165Thr
XM_017003165.2:c.-585A>C	XP_016858654.1:n.-585A>C
NM_006343.3:c.683A>C MANE Select	NP_006334.2:p.Asn228Thr