Canonical Allele Identifier: CA11339127
Gene: MERTK HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17174870

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.111907624C>T , CM000664.2:g.111907624C>T GRCh38
NC_000002.11:g.112665201C>T , CM000664.1:g.112665201C>T GRCh37
NC_000002.10:g.112381672C>T NCBI36
NG_011607.1:g.14011C>T

Transcript Alleles

HGVS Amino-acid change
NM_006343.2:c.61+8828C>T VV NP_006334.2:p.=
XM_005263565.3:c.61+8828C>T XP_005263622.1:p.=
XM_005263568.3:c.61+8828C>T XP_005263625.1:p.=
XM_011510490.1:c.-129+8487C>T XP_011508792.1:p.=
XM_005263565.4:c.61+8828C>T
XM_005263568.4:c.61+8828C>T
XM_011510490.3:c.-129+8487C>T
XM_017003165.2:c.-1207+8828C>T XP_016858654.1:p.=
ENST00000295408.8:c.61+8828C>T ENSP00000295408.4:p.=
ENST00000409780.5:c.-47+8828C>T ENSP00000387277.1:p.=
ENST00000421804.6:c.61+8828C>T ENSP00000389152.2:p.=
ENST00000439966.5:c.61+8828C>T ENSP00000402129.1:p.=
ENST00000616902.4:c.-1155+8828C>T ENSP00000482824.1:p.=