Canonical Allele Identifier: CA1931696686

Gene: CWF19L1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100253432C= , CM000672.2:g.100253432C=	GRCh38
NC_000010.10:g.102013189C= , CM000672.1:g.102013189C=	GRCh37
NC_000010.9:g.102003179C=	NCBI36
NG_041811.1:g.19250G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.612G= MANE Select	ENSP00000326411.6:p.Arg204=
ENST00000354105.8:c.612G=	ENSP00000326411.6:p.Arg204=
ENST00000466955.5:n.169G=
ENST00000468709.5:n.468G=
ENST00000473842.1:n.584G=
ENST00000478047.1:n.1188G=
ENST00000482452.5:n.300G=
ENST00000496796.5:n.376G=
NM_001303404.1:c.612G=	NP_001290333.1:p.Arg204=
NM_001303405.1:c.201G=	NP_001290334.1:p.Arg67=
NM_001303406.1:c.201G=	NP_001290335.1:p.Arg67=
NM_001303407.1:c.-124G=	NP_001290336.1:n.-124G=
NM_018294.5:c.612G=	NP_060764.3:p.Arg204=
NM_018294.6:c.612G= MANE Select	NP_060764.3:p.Arg204=
NM_001303404.2:c.612G=	NP_001290333.1:p.Arg204=
NM_001303405.2:c.201G=	NP_001290334.1:p.Arg67=
NM_001303406.2:c.201G=	NP_001290335.1:p.Arg67=
NM_001303407.2:c.-124G=	NP_001290336.1:n.-124G=