Canonical Allele Identifier: CA2627825125

Gene: CHST14

Linked Data

• gnomAD v4: 15-40472477-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472478dup , CM000677.2:g.40472478dup	GRCh38
NC_000015.9:g.40764677dup , CM000677.1:g.40764677dup	GRCh37
NC_000015.8:g.38551969dup	NCBI36
NG_017074.1:g.6518dup , LRG_600:g.6518dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*134dup MANE Select	ENSP00000307297.6:n.*134dup
ENST00000306243.6:c.*134dup	ENSP00000307297.5:n.*134dup
ENST00000559991.1:c.*134dup	ENSP00000453882.1:n.*134dup
NM_130468.3:c.*134dup , LRG_600t1:c.*134dup	NP_569735.1:n.*134dup
NM_130468.4:c.*134dup MANE Select	NP_569735.1:n.*134dup