Canonical Allele Identifier: CA61602220

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181603962C>T , CM000664.2:g.181603962C>T	GRCh38
NC_000002.11:g.182468689C>T , CM000664.1:g.182468689C>T	GRCh37
NC_000002.10:g.182176934C>T	NCBI36
NG_021178.1:g.58146G>A
NG_021178.2:g.58146G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_201548.5:c.356G>A MANE Select	NP_963842.1:p.Gly119Asp
ENST00000410087.8:c.356G>A MANE Select	ENSP00000386725.3:p.Gly119Asp
NM_001030311.2:c.356G>A	NP_001025482.1:p.Gly119Asp
NM_001030311.3:c.356G>A	NP_001025482.1:p.Gly119Asp
NM_001030312.2:c.356G>A	NP_001025483.1:p.Gly119Asp
NM_001030312.3:c.356G>A	NP_001025483.1:p.Gly119Asp
NM_001030313.2:c.356G>A	NP_001025484.1:p.Gly119Asp
NM_001030313.3:c.356G>A	NP_001025484.1:p.Gly119Asp
NM_001160277.1:c.356G>A	NP_001153749.1:p.Gly119Asp
NM_001160277.2:c.356G>A	NP_001153749.1:p.Gly119Asp
NM_201548.4:c.356G>A	NP_963842.1:p.Gly119Asp
NR_027689.1:n.457G>A
NR_027689.2:n.455G>A
NR_027690.1:n.457G>A
NR_027690.2:n.455G>A
ENST00000339098.9:c.356G>A	ENSP00000341159.5:p.Gly119Asp
ENST00000374967.6:c.356G>A	ENSP00000364106.2:p.Gly119Asp
ENST00000374969.6:c.356G>A	ENSP00000364108.2:p.Gly119Asp
ENST00000374970.6:c.356G>A	ENSP00000364109.2:p.Gly119Asp
ENST00000409440.7:c.356G>A	ENSP00000387080.3:p.Gly119Asp
ENST00000410087.7:c.356G>A	ENSP00000386725.3:p.Gly119Asp
ENST00000421817.5:c.356G>A	ENSP00000411466.1:p.Gly119Asp
ENST00000452174.5:c.356G>A	ENSP00000409198.1:p.Gly119Asp
ENST00000460319.5:n.275G>A
ENST00000466715.5:n.236G>A
ENST00000476070.1:n.255G>A
ENST00000479558.5:n.354G>A
ENST00000494398.5:n.356G>A
ENST00000497337.1:n.497G>A
ENST00000684145.1:c.-337G>A	ENSP00000508396.1:n.-337G>A