Canonical Allele Identifier: CA349740646

Gene: CERKL

Linked Data

• MyVariant Identifiers: chr2:g.182423367T>G (hg19) ; chr2:g.181558640T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558640T>G , CM000664.2:g.181558640T>G	GRCh38
NC_000002.11:g.182423367T>G , CM000664.1:g.182423367T>G	GRCh37
NC_000002.10:g.182131612T>G	NCBI36
NG_021178.1:g.103468A>C
NG_021178.2:g.103468A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-11A>C	ENSP00000508396.1:n.-11A>C
ENST00000410087.8:c.746A>C MANE Select	ENSP00000386725.3:p.Lys249Thr
ENST00000339098.9:c.824A>C	ENSP00000341159.5:p.Lys275Thr
ENST00000374967.6:c.682A>C	ENSP00000364106.2:n.682A>C
ENST00000374969.6:c.482-8932A>C	ENSP00000364108.2:n.482-8932A>C
ENST00000374970.6:c.614-8932A>C	ENSP00000364109.2:n.614-8932A>C
ENST00000409440.7:c.692A>C	ENSP00000387080.3:p.Lys231Thr
ENST00000410087.7:c.746A>C	ENSP00000386725.3:p.Lys249Thr
ENST00000421817.5:c.*28A>C	ENSP00000411466.1:n.*28A>C
ENST00000452174.5:c.550A>C	ENSP00000409198.1:n.550A>C
ENST00000479558.5:n.744A>C
ENST00000494398.5:n.746A>C
NM_001030311.2:c.824A>C	NP_001025482.1:p.Lys275Thr
NM_001030312.2:c.482-8932A>C	NP_001025483.1:n.482-8932A>C
NM_001030313.2:c.614-8932A>C	NP_001025484.1:n.614-8932A>C
NM_001160277.1:c.692A>C	NP_001153749.1:p.Lys231Thr
NM_201548.4:c.746A>C	NP_963842.1:p.Lys249Thr
NR_027689.1:n.651A>C
NR_027690.1:n.783A>C
NM_201548.5:c.746A>C MANE Select	NP_963842.1:p.Lys249Thr
NM_001030311.3:c.824A>C	NP_001025482.1:p.Lys275Thr
NM_001030312.3:c.482-8932A>C	NP_001025483.1:n.482-8932A>C
NM_001030313.3:c.614-8932A>C	NP_001025484.1:n.614-8932A>C
NM_001160277.2:c.692A>C	NP_001153749.1:p.Lys231Thr
NR_027689.2:n.649A>C
NR_027690.2:n.781A>C