Canonical Allele Identifier: CA348242212

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112028371G>A , CM000664.2:g.112028371G>A	GRCh38
NC_000002.11:g.112785948G>A , CM000664.1:g.112785948G>A	GRCh37
NC_000002.10:g.112502419G>A	NCBI36
NG_011607.1:g.134758G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006343.3:c.2507G>A MANE Select	NP_006334.2:p.Cys836Tyr
ENST00000295408.9:c.2507G>A MANE Select	ENSP00000295408.4:p.Cys836Tyr
NM_006343.2:c.2507G>A	NP_006334.2:p.Cys836Tyr
ENST00000295408.8:c.2507G>A	ENSP00000295408.4:p.Cys836Tyr
ENST00000409780.5:c.1979G>A	ENSP00000387277.1:p.Cys660Tyr
ENST00000421804.6:c.2507G>A	ENSP00000389152.2:p.Cys836Tyr
ENST00000439966.5:c.*1980G>A	ENSP00000402129.1:n.*1980G>A
ENST00000449344.2:c.479G>A	ENSP00000412660.2:p.Cys160Tyr
ENST00000616902.4:c.1582G>A	ENSP00000482824.1:p.Ala528Thr
XM_005263565.3:c.2486+5977G>A	XP_005263622.1:n.2486+5977G>A
XM_005263565.4:c.2486+5977G>A	XP_005263622.1:n.2486+5977G>A
XM_011510490.1:c.2318G>A	XP_011508792.1:p.Cys773Tyr
XM_011510490.3:c.2318G>A	XP_011508792.1:p.Cys773Tyr
XM_011510491.1:c.1292G>A	XP_011508793.1:p.Cys431Tyr
XM_017003164.1:c.2318G>A	XP_016858653.1:p.Cys773Tyr
XM_017003165.2:c.1292G>A	XP_016858654.1:p.Cys431Tyr