Canonical Allele Identifier: CA2010863

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181603984G>A , CM000664.2:g.181603984G>A	GRCh38
NC_000002.11:g.182468711G>A , CM000664.1:g.182468711G>A	GRCh37
NC_000002.10:g.182176956G>A	NCBI36
NG_021178.1:g.58124C>T
NG_021178.2:g.58124C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201548.5:c.334C>T MANE Select	NP_963842.1:p.Gln112Ter
ENST00000410087.8:c.334C>T MANE Select	ENSP00000386725.3:p.Gln112Ter
NM_001030311.2:c.334C>T	NP_001025482.1:p.Gln112Ter
NM_001030311.3:c.334C>T	NP_001025482.1:p.Gln112Ter
NM_001030312.2:c.334C>T	NP_001025483.1:p.Gln112Ter
NM_001030312.3:c.334C>T	NP_001025483.1:p.Gln112Ter
NM_001030313.2:c.334C>T	NP_001025484.1:p.Gln112Ter
NM_001030313.3:c.334C>T	NP_001025484.1:p.Gln112Ter
NM_001160277.1:c.334C>T	NP_001153749.1:p.Gln112Ter
NM_001160277.2:c.334C>T	NP_001153749.1:p.Gln112Ter
NM_201548.4:c.334C>T	NP_963842.1:p.Gln112Ter
NR_027689.1:n.435C>T
NR_027689.2:n.433C>T
NR_027690.1:n.435C>T
NR_027690.2:n.433C>T
ENST00000339098.9:c.334C>T	ENSP00000341159.5:p.Gln112Ter
ENST00000374967.6:c.334C>T	ENSP00000364106.2:p.Gln112Ter
ENST00000374969.6:c.334C>T	ENSP00000364108.2:p.Gln112Ter
ENST00000374970.6:c.334C>T	ENSP00000364109.2:p.Gln112Ter
ENST00000409440.7:c.334C>T	ENSP00000387080.3:p.Gln112Ter
ENST00000410087.7:c.334C>T	ENSP00000386725.3:p.Gln112Ter
ENST00000421817.5:c.334C>T	ENSP00000411466.1:p.Gln112Ter
ENST00000452174.5:c.334C>T	ENSP00000409198.1:p.Gln112Ter
ENST00000460319.5:n.253C>T
ENST00000466715.5:n.214C>T
ENST00000476070.1:n.233C>T
ENST00000479558.5:n.332C>T
ENST00000494398.5:n.334C>T
ENST00000497337.1:n.475C>T
ENST00000684145.1:c.-359C>T	ENSP00000508396.1:n.-359C>T