Canonical Allele Identifier: CA1160473283

Gene: CD164L2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.27381437T= , CM000663.2:g.27381437T=	GRCh38
NC_000001.10:g.27707927T= , CM000663.1:g.27707927T=	GRCh37
NC_000001.9:g.27580514T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374030.3:c.373+343A= MANE Select	ENSP00000363142.1:n.373+343A=
ENST00000374027.7:c.373+343A=	ENSP00000363139.3:n.373+343A=
ENST00000374030.2:c.373+343A=	ENSP00000363142.1:n.373+343A=
NM_207397.3:c.373+343A=	NP_997280.2:n.373+343A=
XM_005245868.3:c.373+343A=	XP_005245925.2:n.373+343A=
XM_011541441.1:c.373+343A=	XP_011539743.1:n.373+343A=
XR_241190.3:n.449+343A=
NM_001330448.1:c.373+343A= MANE Select	NP_001317377.1:n.373+343A=
NM_207397.4:c.373+343A=	NP_997280.2:n.373+343A=
NM_207397.5:c.373+343A=	NP_997280.2:n.373+343A=