Canonical Allele Identifier: CA1279526460
Gene: MERTK HGNC NCBI

Linked Data

dbSNP Id: rs1573560974

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111907640G>A , CM000664.2:g.111907640G>A GRCh38
NC_000002.11:g.112665217G>A , CM000664.1:g.112665217G>A GRCh37
NC_000002.10:g.112381688G>A NCBI36
NG_011607.1:g.14027G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000295408.9:c.61+8844G>A MANE Select ENSP00000295408.4:n.61+8844G>A
ENST00000295408.8:c.61+8844G>A ENSP00000295408.4:n.61+8844G>A
ENST00000409780.5:c.-47+8844G>A ENSP00000387277.1:n.-47+8844G>A
ENST00000421804.6:c.61+8844G>A ENSP00000389152.2:n.61+8844G>A
ENST00000439966.5:c.61+8844G>A ENSP00000402129.1:n.61+8844G>A
ENST00000616902.4:c.-1155+8844G>A ENSP00000482824.1:n.-1155+8844G>A
NM_006343.2:c.61+8844G>A NP_006334.2:n.61+8844G>A
XM_005263565.3:c.61+8844G>A XP_005263622.1:n.61+8844G>A
XM_005263568.3:c.61+8844G>A XP_005263625.1:n.61+8844G>A
XM_011510490.1:c.-129+8503G>A XP_011508792.1:n.-129+8503G>A
XM_005263565.4:c.61+8844G>A XP_005263622.1:n.61+8844G>A
XM_005263568.4:c.61+8844G>A XP_005263625.1:n.61+8844G>A
XM_011510490.3:c.-129+8503G>A XP_011508792.1:n.-129+8503G>A
XM_017003165.2:c.-1207+8844G>A XP_016858654.1:n.-1207+8844G>A
NM_006343.3:c.61+8844G>A MANE Select NP_006334.2:n.61+8844G>A