Canonical Allele Identifier: CA1931686303

Gene: CWF19L1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100245820_100245821delinsGA , CM000672.2:g.100245820_100245821delinsGA	GRCh38
NC_000010.10:g.102005577_102005578delinsGA , CM000672.1:g.102005577_102005578delinsGA	GRCh37
NC_000010.9:g.101995567_101995568delinsGA	NCBI36
NG_041811.1:g.26861_26862delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354105.10:c.942_943delinsTC MANE Select	ENSP00000326411.6:p.His314=
ENST00000354105.8:c.942_943delinsTC	ENSP00000326411.6:p.His314=
ENST00000370379.1:c.207_208delinsTC	ENSP00000359405.1:p.His69=
ENST00000466408.1:n.296_297delinsTC
ENST00000466955.5:n.483_484delinsTC
ENST00000468709.5:n.798_799delinsTC
ENST00000478047.1:n.1200-7590_1200-7589delinsTC
ENST00000482452.5:n.630_631delinsTC
ENST00000496796.5:n.706_707delinsTC
NM_001303404.1:c.942_943delinsTC	NP_001290333.1:p.His314=
NM_001303405.1:c.531_532delinsTC	NP_001290334.1:p.His177=
NM_001303406.1:c.531_532delinsTC	NP_001290335.1:p.His177=
NM_001303407.1:c.207_208delinsTC	NP_001290336.1:p.His69=
NM_018294.5:c.942_943delinsTC	NP_060764.3:p.His314=
NM_018294.6:c.942_943delinsTC MANE Select	NP_060764.3:p.His314=
NM_001303404.2:c.942_943delinsTC	NP_001290333.1:p.His314=
NM_001303405.2:c.531_532delinsTC	NP_001290334.1:p.His177=
NM_001303406.2:c.531_532delinsTC	NP_001290335.1:p.His177=
NM_001303407.2:c.207_208delinsTC	NP_001290336.1:p.His69=