Canonical Allele Identifier: CA348231255

Gene: MERTK

Linked Data

• MyVariant Identifiers: chr2:g.112754952T>A (hg19) ; chr2:g.111997375T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997375T>A , CM000664.2:g.111997375T>A	GRCh38
NC_000002.11:g.112754952T>A , CM000664.1:g.112754952T>A	GRCh37
NC_000002.10:g.112471423T>A	NCBI36
NG_011607.1:g.103762T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1503T>A MANE Select	ENSP00000295408.4:p.Pro501=
ENST00000295408.8:c.1503T>A	ENSP00000295408.4:p.Pro501=
ENST00000409780.5:c.975T>A	ENSP00000387277.1:p.Pro325=
ENST00000421804.6:c.1503T>A	ENSP00000389152.2:p.Pro501=
ENST00000439966.5:c.*976T>A	ENSP00000402129.1:n.*976T>A
ENST00000473065.1:n.6T>A
ENST00000616902.4:c.472T>A	ENSP00000482824.1:p.Cys158Ser
NM_006343.2:c.1503T>A	NP_006334.2:p.Pro501=
XM_005263565.3:c.1503T>A	XP_005263622.1:p.Pro501=
XM_005263568.3:c.1503T>A	XP_005263625.1:p.Pro501=
XM_011510490.1:c.1314T>A	XP_011508792.1:p.Pro438=
XM_011510491.1:c.288T>A	XP_011508793.1:p.Pro96=
XM_005263565.4:c.1503T>A	XP_005263622.1:p.Pro501=
XM_005263568.4:c.1503T>A	XP_005263625.1:p.Pro501=
XM_011510490.3:c.1314T>A	XP_011508792.1:p.Pro438=
XM_017003164.1:c.1314T>A	XP_016858653.1:p.Pro438=
XM_017003165.2:c.288T>A	XP_016858654.1:p.Pro96=
NM_006343.3:c.1503T>A MANE Select	NP_006334.2:p.Pro501=