Canonical Allele Identifier: CA2627825176

Gene: CHST14

Linked Data

• gnomAD v4: 15-40472525-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472525G>T , CM000677.2:g.40472525G>T	GRCh38
NC_000015.9:g.40764724G>T , CM000677.1:g.40764724G>T	GRCh37
NC_000015.8:g.38552016G>T	NCBI36
NG_017074.1:g.6565G>T , LRG_600:g.6565G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*181G>T MANE Select	ENSP00000307297.6:n.*181G>T
ENST00000306243.6:c.*181G>T	ENSP00000307297.5:n.*181G>T
ENST00000559991.1:c.*181G>T	ENSP00000453882.1:n.*181G>T
NM_130468.3:c.*181G>T , LRG_600t1:c.*181G>T	NP_569735.1:n.*181G>T
NM_130468.4:c.*181G>T MANE Select	NP_569735.1:n.*181G>T