Canonical Allele Identifier: CA2660687187

Gene: MERTK

Linked Data

• gnomAD v4: 2-111947602-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.111947602C>A , CM000664.2:g.111947602C>A	GRCh38
NC_000002.11:g.112705179C>A , CM000664.1:g.112705179C>A	GRCh37
NC_000002.10:g.112421650C>A	NCBI36
NG_011607.1:g.53989C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295408.9:c.757+35C>A MANE Select	ENSP00000295408.4:n.757+35C>A
ENST00000295408.8:c.757+35C>A	ENSP00000295408.4:n.757+35C>A
ENST00000409780.5:c.229+35C>A	ENSP00000387277.1:n.229+35C>A
ENST00000421804.6:c.757+35C>A	ENSP00000389152.2:n.757+35C>A
ENST00000439966.5:c.*230+35C>A	ENSP00000402129.1:n.*230+35C>A
ENST00000616902.4:c.-459+35C>A	ENSP00000482824.1:n.-459+35C>A
NM_006343.2:c.757+35C>A	NP_006334.2:n.757+35C>A
XM_005263565.3:c.757+35C>A	XP_005263622.1:n.757+35C>A
XM_005263568.3:c.757+35C>A	XP_005263625.1:n.757+35C>A
XM_011510490.1:c.568+35C>A	XP_011508792.1:n.568+35C>A
XM_005263565.4:c.757+35C>A	XP_005263622.1:n.757+35C>A
XM_005263568.4:c.757+35C>A	XP_005263625.1:n.757+35C>A
XM_011510490.3:c.568+35C>A	XP_011508792.1:n.568+35C>A
XM_017003164.1:c.568+35C>A	XP_016858653.1:n.568+35C>A
XM_017003165.2:c.-511+35C>A	XP_016858654.1:n.-511+35C>A
NM_006343.3:c.757+35C>A MANE Select	NP_006334.2:n.757+35C>A