Canonical Allele Identifier: CA2627825198

Gene: CHST14

Linked Data

• gnomAD v4: 15-40472544-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472544C>G , CM000677.2:g.40472544C>G	GRCh38
NC_000015.9:g.40764743C>G , CM000677.1:g.40764743C>G	GRCh37
NC_000015.8:g.38552035C>G	NCBI36
NG_017074.1:g.6584C>G , LRG_600:g.6584C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*200C>G MANE Select	ENSP00000307297.6:n.*200C>G
ENST00000306243.6:c.*200C>G	ENSP00000307297.5:n.*200C>G
ENST00000559991.1:c.*200C>G	ENSP00000453882.1:n.*200C>G
NM_130468.3:c.*200C>G , LRG_600t1:c.*200C>G	NP_569735.1:n.*200C>G
NM_130468.4:c.*200C>G MANE Select	NP_569735.1:n.*200C>G