Canonical Allele Identifier: CA2576064133

Gene: CHST6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479208_75479209insGGG , CM000678.2:g.75479208_75479209insGGG	GRCh38
NC_000016.9:g.75513106_75513107insGGG , CM000678.1:g.75513106_75513107insGGG	GRCh37
NC_000016.8:g.74070607_74070608insGGG	NCBI36
NG_016442.1:g.20820_20821insCCC
NG_016442.2:g.21233_21234insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.620_621insCCC MANE Select	ENSP00000328983.4:p.Val207_Leu208insPro
ENST00000390664.3:c.620_621insCCC	ENSP00000375079.2:p.Val207_Leu208insPro
ENST00000649341.1:c.620_621insCCC	ENSP00000497635.1:p.Val207_Leu208insPro
ENST00000649824.1:c.620_621insCCC	ENSP00000496806.1:p.Val207_Leu208insPro
ENST00000332272.8:c.620_621insCCC	ENSP00000328983.4:p.Val207_Leu208insPro
ENST00000390664.2:c.620_621insCCC	ENSP00000375079.2:p.Val207_Leu208insPro
NM_021615.4:c.620_621insCCC	NP_067628.1:p.Val207_Leu208insPro
XM_005255955.3:c.620_621insCCC	XP_005256012.1:p.Val207_Leu208insPro
XM_011523085.1:c.620_621insCCC	XP_011521387.1:p.Val207_Leu208insPro
NM_021615.5:c.620_621insCCC MANE Select	NP_067628.1:p.Val207_Leu208insPro
XM_005255955.5:c.620_621insCCC	XP_005256012.1:p.Val207_Leu208insPro
XM_011523085.3:c.620_621insCCC	XP_011521387.1:p.Val207_Leu208insPro
NR_163480.1:n.733+2608_733+2609insCCC
NR_163481.1:n.577+2608_577+2609insCCC