Canonical Allele Identifier: CA391762083

Gene: CHST14

Linked Data

• dbSNP Id: rs1555410695
• MyVariant Identifiers: chr15:g.40763485_40763486insC (hg19) ; chr15:g.40471286_40471287insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40471290dup , CM000677.2:g.40471290dup	GRCh38
NC_000015.9:g.40763489dup , CM000677.1:g.40763489dup	GRCh37
NC_000015.8:g.38550781dup	NCBI36
NG_017074.1:g.5330dup , LRG_600:g.5330dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.77dup MANE Select	ENSP00000307297.6:p.Leu27SerfsTer?
ENST00000306243.6:c.77dup	ENSP00000307297.5:p.Leu27SerfsTer?
ENST00000559991.1:c.77dup	ENSP00000453882.1:p.Leu27SerfsTer?
NM_130468.3:c.77dup , LRG_600t1:c.77dup	NP_569735.1:p.Leu27SerfsTer?
NM_130468.4:c.77dup MANE Select	NP_569735.1:p.Leu27SerfsTer?