Canonical Allele Identifier: CA2171795580

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472546_40472549delinsGCTC , CM000677.2:g.40472546_40472549delinsGCTC	GRCh38
NC_000015.9:g.40764745_40764748delinsGCTC , CM000677.1:g.40764745_40764748delinsGCTC	GRCh37
NC_000015.8:g.38552037_38552040delinsGCTC	NCBI36
NG_017074.1:g.6586_6589delinsGCTC , LRG_600:g.6586_6589delinsGCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*202_*205delinsGCTC MANE Select	ENSP00000307297.6:n.*202_*205delinsGCTC
ENST00000306243.6:c.*202_*205delinsGCTC	ENSP00000307297.5:n.*202_*205delinsGCTC
ENST00000559991.1:c.*202_*205delinsGCTC	ENSP00000453882.1:n.*202_*205delinsGCTC
NM_130468.3:c.*202_*205delinsGCTC , LRG_600t1:c.*202_*205delinsGCTC	NP_569735.1:n.*202_*205delinsGCTC
NM_130468.4:c.*202_*205delinsGCTC MANE Select	NP_569735.1:n.*202_*205delinsGCTC