Canonical Allele Identifier: CA655885232

Gene: CHST14

Linked Data

• COSMIC: COSN26696375

Genomic Alleles

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

Transcript Alleles

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