Canonical Allele Identifier: CA348226650

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112687033A>C (hg19) ; chr2:g.111929456A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111929456A>C , CM000664.2:g.111929456A>C	GRCh38
NC_000002.11:g.112687033A>C , CM000664.1:g.112687033A>C	GRCh37
NC_000002.10:g.112403504A>C	NCBI36
NG_011607.1:g.35843A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.398A>C MANE Select	ENSP00000295408.4:p.Asp133Ala
ENST00000295408.8:c.398A>C	ENSP00000295408.4:p.Asp133Ala
ENST00000409780.5:c.-46-15504A>C	ENSP00000387277.1:n.-46-15504A>C
ENST00000421804.6:c.398A>C	ENSP00000389152.2:p.Asp133Ala
ENST00000439966.5:c.246+152A>C	ENSP00000402129.1:n.246+152A>C
ENST00000616902.4:c.-818A>C	ENSP00000482824.1:n.-818A>C
NM_006343.2:c.398A>C	NP_006334.2:p.Asp133Ala
XM_005263565.3:c.398A>C	XP_005263622.1:p.Asp133Ala
XM_005263568.3:c.398A>C	XP_005263625.1:p.Asp133Ala
XM_011510490.1:c.209A>C	XP_011508792.1:p.Asp70Ala
XM_005263565.4:c.398A>C	XP_005263622.1:p.Asp133Ala
XM_005263568.4:c.398A>C	XP_005263625.1:p.Asp133Ala
XM_011510490.3:c.209A>C	XP_011508792.1:p.Asp70Ala
XM_017003164.1:c.209A>C	XP_016858653.1:p.Asp70Ala
XM_017003165.2:c.-870A>C	XP_016858654.1:n.-870A>C
NM_006343.3:c.398A>C MANE Select	NP_006334.2:p.Asp133Ala