Canonical Allele Identifier: CA2295872752

Gene: C18orf21

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.35977503A= , CM000680.2:g.35977503A=	GRCh38
NC_000018.9:g.33557466A= , CM000680.1:g.33557466A=	GRCh37
NC_000018.8:g.31811464A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_031446.5:c.394A= MANE Select	NP_113634.3:p.Thr132=
ENST00000592875.6:c.394A= MANE Select	ENSP00000465517.1:p.Thr132=
NM_001201474.1:c.130A=	NP_001188403.1:p.Thr44=
NM_001201474.2:c.130A=	NP_001188403.1:p.Thr44=
NM_001201475.1:c.130A=	NP_001188404.1:p.Thr44=
NM_001201475.2:c.130A=	NP_001188404.1:p.Thr44=
NM_001201476.1:c.301-1332A=	NP_001188405.1:n.301-1332A=
NM_001201476.2:c.301-1332A=	NP_001188405.1:n.301-1332A=
NM_031446.4:c.394A=	NP_113634.3:p.Thr132=
ENST00000269194.10:c.130A=	ENSP00000269194.6:p.Thr44=
ENST00000333234.5:c.130A=	ENSP00000329492.5:p.Thr44=
ENST00000587873.5:c.130A=	ENSP00000466400.1:p.Thr44=
ENST00000592875.5:c.394A=	ENSP00000465517.1:p.Thr132=
ENST00000610527.4:c.130A=	ENSP00000480486.1:p.Thr44=
ENST00000618334.1:c.301-1332A=	ENSP00000483334.1:n.301-1332A=
XM_005258364.3:c.412A=	XP_005258421.1:p.Thr138=
XM_005258364.5:c.412A=	XP_005258421.1:p.Thr138=