Canonical Allele Identifier: CA2739770874

Gene: MERTK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111997256T>G , CM000664.2:g.111997256T>G	GRCh38
NC_000002.11:g.112754833T>G , CM000664.1:g.112754833T>G	GRCh37
NC_000002.10:g.112471304T>G	NCBI36
NG_011607.1:g.103643T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.1451-67T>G MANE Select	ENSP00000295408.4:n.1451-67T>G
ENST00000295408.8:c.1451-67T>G	ENSP00000295408.4:n.1451-67T>G
ENST00000409780.5:c.923-67T>G	ENSP00000387277.1:n.923-67T>G
ENST00000421804.6:c.1451-67T>G	ENSP00000389152.2:n.1451-67T>G
ENST00000439966.5:c.*924-67T>G	ENSP00000402129.1:n.*924-67T>G
ENST00000616902.4:c.408T>G	ENSP00000482824.1:p.Leu136=
NM_006343.2:c.1451-67T>G	NP_006334.2:n.1451-67T>G
XM_005263565.3:c.1451-67T>G	XP_005263622.1:n.1451-67T>G
XM_005263568.3:c.1451-67T>G	XP_005263625.1:n.1451-67T>G
XM_011510490.1:c.1262-67T>G	XP_011508792.1:n.1262-67T>G
XM_011510491.1:c.236-67T>G	XP_011508793.1:n.236-67T>G
XM_005263565.4:c.1451-67T>G	XP_005263622.1:n.1451-67T>G
XM_005263568.4:c.1451-67T>G	XP_005263625.1:n.1451-67T>G
XM_011510490.3:c.1262-67T>G	XP_011508792.1:n.1262-67T>G
XM_017003164.1:c.1262-67T>G	XP_016858653.1:n.1262-67T>G
XM_017003165.2:c.236-67T>G	XP_016858654.1:n.236-67T>G
NM_006343.3:c.1451-67T>G MANE Select	NP_006334.2:n.1451-67T>G