Canonical Allele Identifier: CA349740910
Gene: CERKL HGNC NCBI

Linked Data

dbSNP Id: rs1688310170

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181558668C>T , CM000664.2:g.181558668C>T GRCh38
NC_000002.11:g.182423395C>T , CM000664.1:g.182423395C>T GRCh37
NC_000002.10:g.182131640C>T NCBI36
NG_021178.1:g.103440G>A
NG_021178.2:g.103440G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684145.1:c.-39G>A ENSP00000508396.1:n.-39G>A
ENST00000410087.8:c.718G>A MANE Select ENSP00000386725.3:p.Ala240Thr
ENST00000339098.9:c.796G>A ENSP00000341159.5:p.Ala266Thr
ENST00000374967.6:c.654G>A ENSP00000364106.2:p.Ter218=
ENST00000374969.6:c.482-8960G>A ENSP00000364108.2:n.482-8960G>A
ENST00000374970.6:c.614-8960G>A ENSP00000364109.2:n.614-8960G>A
ENST00000409440.7:c.664G>A ENSP00000387080.3:p.Ala222Thr
ENST00000410087.7:c.718G>A ENSP00000386725.3:p.Ala240Thr
ENST00000421817.5:c.522G>A ENSP00000411466.1:p.Ter174=
ENST00000452174.5:c.522G>A ENSP00000409198.1:p.Ter174=
ENST00000466715.5:n.534G>A
ENST00000479558.5:n.716G>A
ENST00000494398.5:n.718G>A
NM_001030311.2:c.796G>A NP_001025482.1:p.Ala266Thr
NM_001030312.2:c.482-8960G>A NP_001025483.1:n.482-8960G>A
NM_001030313.2:c.614-8960G>A NP_001025484.1:n.614-8960G>A
NM_001160277.1:c.664G>A NP_001153749.1:p.Ala222Thr
NM_201548.4:c.718G>A NP_963842.1:p.Ala240Thr
NR_027689.1:n.623G>A
NR_027690.1:n.755G>A
NM_201548.5:c.718G>A MANE Select NP_963842.1:p.Ala240Thr
NM_001030311.3:c.796G>A NP_001025482.1:p.Ala266Thr
NM_001030312.3:c.482-8960G>A NP_001025483.1:n.482-8960G>A
NM_001030313.3:c.614-8960G>A NP_001025484.1:n.614-8960G>A
NM_001160277.2:c.664G>A NP_001153749.1:p.Ala222Thr
NR_027689.2:n.621G>A
NR_027690.2:n.753G>A