Canonical Allele Identifier: CA2634344664

Gene: CHST6

Linked Data

• gnomAD v4: 16-75479209-ACGGCCCGCGGGTCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479212_75479225del , CM000678.2:g.75479212_75479225del	GRCh38
NC_000016.9:g.75513110_75513123del , CM000678.1:g.75513110_75513123del	GRCh37
NC_000016.8:g.74070611_74070624del	NCBI36
NG_016442.1:g.20806_20819del
NG_016442.2:g.21219_21232del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.606_619del MANE Select	ENSP00000328983.4:p.Asp203AlafsTer14
ENST00000390664.3:c.606_619del	ENSP00000375079.2:p.Asp203AlafsTer14
ENST00000649341.1:c.606_619del	ENSP00000497635.1:p.Asp203AlafsTer14
ENST00000649824.1:c.606_619del	ENSP00000496806.1:p.Asp203AlafsTer14
ENST00000332272.8:c.606_619del	ENSP00000328983.4:p.Asp203AlafsTer14
ENST00000390664.2:c.606_619del	ENSP00000375079.2:p.Asp203AlafsTer14
NM_021615.4:c.606_619del	NP_067628.1:p.Asp203AlafsTer14
XM_005255955.3:c.606_619del	XP_005256012.1:p.Asp203AlafsTer14
XM_011523085.1:c.606_619del	XP_011521387.1:p.Asp203AlafsTer14
NM_021615.5:c.606_619del MANE Select	NP_067628.1:p.Asp203AlafsTer14
XM_005255955.5:c.606_619del	XP_005256012.1:p.Asp203AlafsTer14
XM_011523085.3:c.606_619del	XP_011521387.1:p.Asp203AlafsTer14
NR_163480.1:n.733+2594_733+2607del
NR_163481.1:n.577+2594_577+2607del