Canonical Allele Identifier: CA428274350

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112755045A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997468A>T , CM000664.2:g.111997468A>T	GRCh38
NC_000002.11:g.112755045A>T , CM000664.1:g.112755045A>T	GRCh37
NC_000002.10:g.112471516A>T	NCBI36
NG_011607.1:g.103855A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1596A>T MANE Select	ENSP00000295408.4:p.Thr532=
ENST00000295408.8:c.1596A>T	ENSP00000295408.4:p.Thr532=
ENST00000409780.5:c.1068A>T	ENSP00000387277.1:p.Thr356=
ENST00000421804.6:c.1596A>T	ENSP00000389152.2:p.Thr532=
ENST00000439966.5:c.*1069A>T	ENSP00000402129.1:n.*1069A>T
ENST00000473065.1:n.99A>T
ENST00000616902.4:c.561A>T	ENSP00000482824.1:p.Thr187=
NM_006343.2:c.1596A>T	NP_006334.2:p.Thr532=
XM_005263565.3:c.1596A>T	XP_005263622.1:p.Thr532=
XM_005263568.3:c.1596A>T	XP_005263625.1:p.Thr532=
XM_011510490.1:c.1407A>T	XP_011508792.1:p.Thr469=
XM_011510491.1:c.381A>T	XP_011508793.1:p.Thr127=
XM_005263565.4:c.1596A>T	XP_005263622.1:p.Thr532=
XM_005263568.4:c.1596A>T	XP_005263625.1:p.Thr532=
XM_011510490.3:c.1407A>T	XP_011508792.1:p.Thr469=
XM_017003164.1:c.1407A>T	XP_016858653.1:p.Thr469=
XM_017003165.2:c.381A>T	XP_016858654.1:p.Thr127=
NM_006343.3:c.1596A>T MANE Select	NP_006334.2:p.Thr532=