Canonical Allele Identifier: CA61583218

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181548605C>G , CM000664.2:g.181548605C>G	GRCh38
NC_000002.11:g.182413332C>G , CM000664.1:g.182413332C>G	GRCh37
NC_000002.10:g.182121577C>G	NCBI36
NG_021178.1:g.113503G>C
NG_021178.2:g.113503G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_201548.5:c.1074-1G>C MANE Select	NP_963842.1:n.1074-1G>C
ENST00000410087.8:c.1074-1G>C MANE Select	ENSP00000386725.3:n.1074-1G>C
NM_001030311.2:c.1152-1G>C	NP_001025482.1:n.1152-1G>C
NM_001030311.3:c.1152-1G>C	NP_001025482.1:n.1152-1G>C
NM_001030312.2:c.735-1G>C	NP_001025483.1:n.735-1G>C
NM_001030312.3:c.735-1G>C	NP_001025483.1:n.735-1G>C
NM_001030313.2:c.867-1G>C	NP_001025484.1:n.867-1G>C
NM_001030313.3:c.867-1G>C	NP_001025484.1:n.867-1G>C
NM_001160277.1:c.1020-1G>C	NP_001153749.1:n.1020-1G>C
NM_001160277.2:c.1020-1G>C	NP_001153749.1:n.1020-1G>C
NM_201548.4:c.1074-1G>C	NP_963842.1:n.1074-1G>C
NR_027689.1:n.979-1G>C
NR_027689.2:n.977-1G>C
NR_027690.1:n.1111-1G>C
NR_027690.2:n.1109-1G>C
ENST00000339098.9:c.1152-1G>C	ENSP00000341159.5:n.1152-1G>C
ENST00000374967.6:c.1010-1G>C	ENSP00000364106.2:n.1010-1G>C
ENST00000374969.6:c.735-1G>C	ENSP00000364108.2:n.735-1G>C
ENST00000374970.6:c.867-1G>C	ENSP00000364109.2:n.867-1G>C
ENST00000409440.7:c.1020-1G>C	ENSP00000387080.3:n.1020-1G>C
ENST00000410087.7:c.1074-1G>C	ENSP00000386725.3:n.1074-1G>C
ENST00000421817.5:c.*356-1G>C	ENSP00000411466.1:n.*356-1G>C
ENST00000452174.5:c.878-1G>C	ENSP00000409198.1:n.878-1G>C
ENST00000479558.5:n.1072-1G>C
ENST00000494398.5:n.1074-1G>C
ENST00000684145.1:c.318-1G>C	ENSP00000508396.1:n.318-1G>C