Canonical Allele Identifier: CA428548136

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112687103A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111929526A>C , CM000664.2:g.111929526A>C	GRCh38
NC_000002.11:g.112687103A>C , CM000664.1:g.112687103A>C	GRCh37
NC_000002.10:g.112403574A>C	NCBI36
NG_011607.1:g.35913A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.468A>C MANE Select	ENSP00000295408.4:p.Ile156=
ENST00000295408.8:c.468A>C	ENSP00000295408.4:p.Ile156=
ENST00000409780.5:c.-46-15434A>C	ENSP00000387277.1:n.-46-15434A>C
ENST00000421804.6:c.468A>C	ENSP00000389152.2:p.Ile156=
ENST00000439966.5:c.246+222A>C	ENSP00000402129.1:n.246+222A>C
ENST00000616902.4:c.-748A>C	ENSP00000482824.1:n.-748A>C
NM_006343.2:c.468A>C	NP_006334.2:p.Ile156=
XM_005263565.3:c.468A>C	XP_005263622.1:p.Ile156=
XM_005263568.3:c.468A>C	XP_005263625.1:p.Ile156=
XM_011510490.1:c.279A>C	XP_011508792.1:p.Ile93=
XM_005263565.4:c.468A>C	XP_005263622.1:p.Ile156=
XM_005263568.4:c.468A>C	XP_005263625.1:p.Ile156=
XM_011510490.3:c.279A>C	XP_011508792.1:p.Ile93=
XM_017003164.1:c.279A>C	XP_016858653.1:p.Ile93=
XM_017003165.2:c.-800A>C	XP_016858654.1:n.-800A>C
NM_006343.3:c.468A>C MANE Select	NP_006334.2:p.Ile156=