Canonical Allele Identifier: CA1931677149

Gene: CWF19L1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100237955A= , CM000672.2:g.100237955A=	GRCh38
NC_000010.10:g.101997712A= , CM000672.1:g.101997712A=	GRCh37
NC_000010.9:g.101987702A=	NCBI36
NG_041811.1:g.34727T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.1254+67T= MANE Select	ENSP00000326411.6:n.1254+67T=
ENST00000354105.8:c.1254+67T=	ENSP00000326411.6:n.1254+67T=
ENST00000370379.1:c.519+67T=	ENSP00000359405.1:n.519+67T=
ENST00000468709.5:n.1110+67T=
ENST00000478047.1:n.1409+67T=
ENST00000482452.5:n.937+67T=
NM_001303404.1:c.1254+67T=	NP_001290333.1:n.1254+67T=
NM_001303405.1:c.843+67T=	NP_001290334.1:n.843+67T=
NM_001303406.1:c.843+67T=	NP_001290335.1:n.843+67T=
NM_001303407.1:c.519+67T=	NP_001290336.1:n.519+67T=
NM_018294.5:c.1254+67T=	NP_060764.3:n.1254+67T=
NM_018294.6:c.1254+67T= MANE Select	NP_060764.3:n.1254+67T=
NM_001303404.2:c.1254+67T=	NP_001290333.1:n.1254+67T=
NM_001303405.2:c.843+67T=	NP_001290334.1:n.843+67T=
NM_001303406.2:c.843+67T=	NP_001290335.1:n.843+67T=
NM_001303407.2:c.519+67T=	NP_001290336.1:n.519+67T=