Canonical Allele Identifier: CA2627825127

Gene: CHST14

Linked Data

• gnomAD v4: 15-40472485-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472487del , CM000677.2:g.40472487del	GRCh38
NC_000015.9:g.40764686del , CM000677.1:g.40764686del	GRCh37
NC_000015.8:g.38551978del	NCBI36
NG_017074.1:g.6527del , LRG_600:g.6527del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*143del MANE Select	ENSP00000307297.6:n.*143del
ENST00000306243.6:c.*143del	ENSP00000307297.5:n.*143del
ENST00000559991.1:c.*143del	ENSP00000453882.1:n.*143del
NM_130468.3:c.*143del , LRG_600t1:c.*143del	NP_569735.1:n.*143del
NM_130468.4:c.*143del MANE Select	NP_569735.1:n.*143del