Canonical Allele Identifier: CA2627825133

Gene: CHST14

Linked Data

• gnomAD v4: 15-40472491-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472493del , CM000677.2:g.40472493del	GRCh38
NC_000015.9:g.40764692del , CM000677.1:g.40764692del	GRCh37
NC_000015.8:g.38551984del	NCBI36
NG_017074.1:g.6533del , LRG_600:g.6533del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*149del MANE Select	ENSP00000307297.6:n.*149del
ENST00000306243.6:c.*149del	ENSP00000307297.5:n.*149del
ENST00000559991.1:c.*149del	ENSP00000453882.1:n.*149del
NM_130468.3:c.*149del , LRG_600t1:c.*149del	NP_569735.1:n.*149del
NM_130468.4:c.*149del MANE Select	NP_569735.1:n.*149del