Canonical Allele Identifier: CA349733510

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181539265C>A , CM000664.2:g.181539265C>A	GRCh38
NC_000002.11:g.182403992C>A , CM000664.1:g.182403992C>A	GRCh37
NC_000002.10:g.182112237C>A	NCBI36
NG_021178.1:g.122843G>T
NG_050623.1:g.87374C>A
NG_021178.2:g.122843G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201548.5:c.1366-1G>T MANE Select	NP_963842.1:n.1366-1G>T
ENST00000410087.8:c.1366-1G>T MANE Select	ENSP00000386725.3:n.1366-1G>T
NM_001030311.2:c.1444-1G>T	NP_001025482.1:n.1444-1G>T
NM_001030311.3:c.1444-1G>T	NP_001025482.1:n.1444-1G>T
NM_001030312.2:c.1027-1G>T	NP_001025483.1:n.1027-1G>T
NM_001030312.3:c.1027-1G>T	NP_001025483.1:n.1027-1G>T
NM_001030313.2:c.1159-1G>T	NP_001025484.1:n.1159-1G>T
NM_001030313.3:c.1159-1G>T	NP_001025484.1:n.1159-1G>T
NM_001160277.1:c.1312-1G>T	NP_001153749.1:n.1312-1G>T
NM_001160277.2:c.1312-1G>T	NP_001153749.1:n.1312-1G>T
NM_201548.4:c.1366-1G>T	NP_963842.1:n.1366-1G>T
NR_027689.1:n.1271-1G>T
NR_027689.2:n.1269-1G>T
NR_027690.1:n.1403-1G>T
NR_027690.2:n.1401-1G>T
ENST00000339098.9:c.1444-1G>T	ENSP00000341159.5:n.1444-1G>T
ENST00000374967.6:c.1302-1G>T	ENSP00000364106.2:n.1302-1G>T
ENST00000374969.6:c.1027-1G>T	ENSP00000364108.2:n.1027-1G>T
ENST00000374970.6:c.1159-1G>T	ENSP00000364109.2:n.1159-1G>T
ENST00000409440.7:c.1312-1G>T	ENSP00000387080.3:n.1312-1G>T
ENST00000410087.7:c.1366-1G>T	ENSP00000386725.3:n.1366-1G>T
ENST00000421817.5:c.*622-1G>T	ENSP00000411466.1:n.*622-1G>T
ENST00000452174.5:c.1170-1G>T	ENSP00000409198.1:n.1170-1G>T
ENST00000494398.5:n.2158-1G>T
ENST00000684145.1:c.610-1G>T	ENSP00000508396.1:n.610-1G>T