Canonical Allele Identifier: CA349720546

Gene: CWC22

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.179945387T>A , CM000664.2:g.179945387T>A	GRCh38
NC_000002.11:g.180810114T>A , CM000664.1:g.180810114T>A	GRCh37
NC_000002.10:g.180518359T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410053.8:c.2469A>T MANE Select	ENSP00000387006.3:p.Arg823Ser
ENST00000410053.7:c.2469A>T	ENSP00000387006.3:p.Arg823Ser
NM_020943.2:c.2469A>T	NP_065994.1:p.Arg823Ser
XM_005246726.1:c.2469A>T	XP_005246783.1:p.Arg823Ser
XM_005246726.3:c.2469A>T	XP_005246783.1:p.Arg823Ser
NM_020943.3:c.2469A>T MANE Select	NP_065994.1:p.Arg823Ser
NM_001376029.1:c.2469A>T	NP_001362958.1:p.Arg823Ser
NM_001376030.1:c.2469A>T	NP_001362959.1:p.Arg823Ser
NM_001376032.1:c.2346A>T	NP_001362961.1:p.Arg782Ser
NM_001376033.1:c.*325A>T	NP_001362962.1:n.*325A>T