Canonical Allele Identifier: CA1931686323

Gene: CWF19L1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245822_100245825delinsTGAG , CM000672.2:g.100245822_100245825delinsTGAG	GRCh38
NC_000010.10:g.102005579_102005582delinsTGAG , CM000672.1:g.102005579_102005582delinsTGAG	GRCh37
NC_000010.9:g.101995569_101995572delinsTGAG	NCBI36
NG_041811.1:g.26857_26860delinsCTCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000354105.10:c.938_941delinsCTCA MANE Select	ENSP00000326411.6:p.Pro313=
ENST00000354105.8:c.938_941delinsCTCA	ENSP00000326411.6:p.Pro313=
ENST00000370379.1:c.203_206delinsCTCA	ENSP00000359405.1:p.Pro68=
ENST00000466408.1:n.292_295delinsCTCA
ENST00000466955.5:n.479_482delinsCTCA
ENST00000468709.5:n.794_797delinsCTCA
ENST00000478047.1:n.1200-7594_1200-7591delinsCTCA
ENST00000482452.5:n.626_629delinsCTCA
ENST00000496796.5:n.702_705delinsCTCA
NM_001303404.1:c.938_941delinsCTCA	NP_001290333.1:p.Pro313=
NM_001303405.1:c.527_530delinsCTCA	NP_001290334.1:p.Pro176=
NM_001303406.1:c.527_530delinsCTCA	NP_001290335.1:p.Pro176=
NM_001303407.1:c.203_206delinsCTCA	NP_001290336.1:p.Pro68=
NM_018294.5:c.938_941delinsCTCA	NP_060764.3:p.Pro313=
NM_018294.6:c.938_941delinsCTCA MANE Select	NP_060764.3:p.Pro313=
NM_001303404.2:c.938_941delinsCTCA	NP_001290333.1:p.Pro313=
NM_001303405.2:c.527_530delinsCTCA	NP_001290334.1:p.Pro176=
NM_001303406.2:c.527_530delinsCTCA	NP_001290335.1:p.Pro176=
NM_001303407.2:c.203_206delinsCTCA	NP_001290336.1:p.Pro68=