Canonical Allele Identifier: CA61802990

Gene: CWC22

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.179973206A>G , CM000664.2:g.179973206A>G	GRCh38
NC_000002.11:g.180837933A>G , CM000664.1:g.180837933A>G	GRCh37
NC_000002.10:g.180546178A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410053.8:c.791T>C MANE Select	ENSP00000387006.3:p.Ile264Thr
ENST00000404136.2:c.791T>C	ENSP00000384159.2:p.Ile264Thr
ENST00000410053.7:c.791T>C	ENSP00000387006.3:p.Ile264Thr
NM_020943.2:c.791T>C	NP_065994.1:p.Ile264Thr
XM_005246726.1:c.791T>C	XP_005246783.1:p.Ile264Thr
XM_005246726.3:c.791T>C	XP_005246783.1:p.Ile264Thr
NM_020943.3:c.791T>C MANE Select	NP_065994.1:p.Ile264Thr
NM_001376029.1:c.791T>C	NP_001362958.1:p.Ile264Thr
NM_001376030.1:c.791T>C	NP_001362959.1:p.Ile264Thr
NM_001376032.1:c.668T>C	NP_001362961.1:p.Ile223Thr
NM_001376033.1:c.791T>C	NP_001362962.1:p.Ile264Thr