Canonical Allele Identifier: CA2575679829

Gene: CHST14

Linked Data

• gnomAD v4: 15-40472400-GCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472403_40472405del , CM000677.2:g.40472403_40472405del	GRCh38
NC_000015.9:g.40764602_40764604del , CM000677.1:g.40764602_40764604del	GRCh37
NC_000015.8:g.38551894_38551896del	NCBI36
NG_017074.1:g.6443_6445del , LRG_600:g.6443_6445del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*59_*61del MANE Select	ENSP00000307297.6:n.*59_*61del
ENST00000306243.6:c.*59_*61del	ENSP00000307297.5:n.*59_*61del
ENST00000559991.1:c.*59_*61del	ENSP00000453882.1:n.*59_*61del
NM_130468.3:c.*59_*61del , LRG_600t1:c.*59_*61del	NP_569735.1:n.*59_*61del
NM_130468.4:c.*59_*61del MANE Select	NP_569735.1:n.*59_*61del