Canonical Allele Identifier: CA1160473279
Gene: CD164L2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.27381433G= , CM000663.2:g.27381433G= GRCh38
NC_000001.10:g.27707923G= , CM000663.1:g.27707923G= GRCh37
NC_000001.9:g.27580510G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374030.3:c.373+347C= MANE Select ENSP00000363142.1:n.373+347C=
ENST00000374027.7:c.373+347C= ENSP00000363139.3:n.373+347C=
ENST00000374030.2:c.373+347C= ENSP00000363142.1:n.373+347C=
NM_207397.3:c.373+347C= NP_997280.2:n.373+347C=
XM_005245868.3:c.373+347C= XP_005245925.2:n.373+347C=
XM_011541441.1:c.373+347C= XP_011539743.1:n.373+347C=
XR_241190.3:n.449+347C=
NM_001330448.1:c.373+347C= MANE Select NP_001317377.1:n.373+347C=
NM_207397.4:c.373+347C= NP_997280.2:n.373+347C=
NM_207397.5:c.373+347C= NP_997280.2:n.373+347C=