Canonical Allele Identifier: CA1311924596
Gene: CERKL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181558618G= , CM000664.2:g.181558618G= GRCh38
NC_000002.11:g.182423345G= , CM000664.1:g.182423345G= GRCh37
NC_000002.10:g.182131590G= NCBI36
NG_021178.1:g.103490C=
NG_021178.2:g.103490C=

Transcript Alleles

HGVS Amino-acid change
ENST00000684145.1:c.12C= ENSP00000508396.1:p.Asp4=
ENST00000410087.8:c.768C= MANE Select ENSP00000386725.3:p.Asp256=
ENST00000339098.9:c.846C= ENSP00000341159.5:p.Asp282=
ENST00000374967.6:c.704C= ENSP00000364106.2:n.704C=
ENST00000374969.6:c.482-8910C= ENSP00000364108.2:n.482-8910C=
ENST00000374970.6:c.614-8910C= ENSP00000364109.2:n.614-8910C=
ENST00000409440.7:c.714C= ENSP00000387080.3:p.Asp238=
ENST00000410087.7:c.768C= ENSP00000386725.3:p.Asp256=
ENST00000421817.5:c.*50C= ENSP00000411466.1:n.*50C=
ENST00000452174.5:c.572C= ENSP00000409198.1:n.572C=
ENST00000479558.5:n.766C=
ENST00000494398.5:n.768C=
NM_001030311.2:c.846C= NP_001025482.1:p.Asp282=
NM_001030312.2:c.482-8910C= NP_001025483.1:n.482-8910C=
NM_001030313.2:c.614-8910C= NP_001025484.1:n.614-8910C=
NM_001160277.1:c.714C= NP_001153749.1:p.Asp238=
NM_201548.4:c.768C= NP_963842.1:p.Asp256=
NR_027689.1:n.673C=
NR_027690.1:n.805C=
NM_201548.5:c.768C= MANE Select NP_963842.1:p.Asp256=
NM_001030311.3:c.846C= NP_001025482.1:p.Asp282=
NM_001030312.3:c.482-8910C= NP_001025483.1:n.482-8910C=
NM_001030313.3:c.614-8910C= NP_001025484.1:n.614-8910C=
NM_001160277.2:c.714C= NP_001153749.1:p.Asp238=
NR_027689.2:n.671C=
NR_027690.2:n.803C=