Canonical Allele Identifier: CA61783395

Gene: CWC22

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.179952505C>G , CM000664.2:g.179952505C>G	GRCh38
NC_000002.11:g.180817232C>G , CM000664.1:g.180817232C>G	GRCh37
NC_000002.10:g.180525477C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410053.8:c.1783G>C MANE Select	ENSP00000387006.3:p.Gly595Arg
ENST00000404136.2:c.1783G>C	ENSP00000384159.2:p.Gly595Arg
ENST00000410053.7:c.1783G>C	ENSP00000387006.3:p.Gly595Arg
NM_020943.2:c.1783G>C	NP_065994.1:p.Gly595Arg
XM_005246726.1:c.1783G>C	XP_005246783.1:p.Gly595Arg
XM_005246726.3:c.1783G>C	XP_005246783.1:p.Gly595Arg
NM_020943.3:c.1783G>C MANE Select	NP_065994.1:p.Gly595Arg
NM_001376029.1:c.1783G>C	NP_001362958.1:p.Gly595Arg
NM_001376030.1:c.1783G>C	NP_001362959.1:p.Gly595Arg
NM_001376032.1:c.1660G>C	NP_001362961.1:p.Gly554Arg
NM_001376033.1:c.1783G>C	NP_001362962.1:p.Gly595Arg