Canonical Allele Identifier: CA428270398

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112705113T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947536T>G , CM000664.2:g.111947536T>G	GRCh38
NC_000002.11:g.112705113T>G , CM000664.1:g.112705113T>G	GRCh37
NC_000002.10:g.112421584T>G	NCBI36
NG_011607.1:g.53923T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.726T>G MANE Select	ENSP00000295408.4:p.Pro242=
ENST00000295408.8:c.726T>G	ENSP00000295408.4:p.Pro242=
ENST00000409780.5:c.198T>G	ENSP00000387277.1:p.Pro66=
ENST00000421804.6:c.726T>G	ENSP00000389152.2:p.Pro242=
ENST00000439966.5:c.*199T>G	ENSP00000402129.1:n.*199T>G
ENST00000616902.4:c.-490T>G	ENSP00000482824.1:n.-490T>G
NM_006343.2:c.726T>G	NP_006334.2:p.Pro242=
XM_005263565.3:c.726T>G	XP_005263622.1:p.Pro242=
XM_005263568.3:c.726T>G	XP_005263625.1:p.Pro242=
XM_011510490.1:c.537T>G	XP_011508792.1:p.Pro179=
XM_005263565.4:c.726T>G	XP_005263622.1:p.Pro242=
XM_005263568.4:c.726T>G	XP_005263625.1:p.Pro242=
XM_011510490.3:c.537T>G	XP_011508792.1:p.Pro179=
XM_017003164.1:c.537T>G	XP_016858653.1:p.Pro179=
XM_017003165.2:c.-542T>G	XP_016858654.1:n.-542T>G
NM_006343.3:c.726T>G MANE Select	NP_006334.2:p.Pro242=