Canonical Allele Identifier: CA2233372514

Gene: CHST6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479240_75479251delinsTGCGTAGGTTGA , CM000678.2:g.75479240_75479251delinsTGCGTAGGTTGA	GRCh38
NC_000016.9:g.75513138_75513149delinsTGCGTAGGTTGA , CM000678.1:g.75513138_75513149delinsTGCGTAGGTTGA	GRCh37
NC_000016.8:g.74070639_74070650delinsTGCGTAGGTTGA	NCBI36
NG_016442.1:g.20778_20789delinsTCAACCTACGCA
NG_016442.2:g.21191_21202delinsTCAACCTACGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.578_589delinsTCAACCTACGCA MANE Select	ENSP00000328983.4:p.Leu193=
ENST00000390664.3:c.578_589delinsTCAACCTACGCA	ENSP00000375079.2:p.Leu193=
ENST00000649341.1:c.578_589delinsTCAACCTACGCA	ENSP00000497635.1:p.Leu193=
ENST00000649824.1:c.578_589delinsTCAACCTACGCA	ENSP00000496806.1:p.Leu193=
ENST00000332272.8:c.578_589delinsTCAACCTACGCA	ENSP00000328983.4:p.Leu193=
ENST00000390664.2:c.578_589delinsTCAACCTACGCA	ENSP00000375079.2:p.Leu193=
NM_021615.4:c.578_589delinsTCAACCTACGCA	NP_067628.1:p.Leu193=
XM_005255955.3:c.578_589delinsTCAACCTACGCA	XP_005256012.1:p.Leu193=
XM_011523085.1:c.578_589delinsTCAACCTACGCA	XP_011521387.1:p.Leu193=
NM_021615.5:c.578_589delinsTCAACCTACGCA MANE Select	NP_067628.1:p.Leu193=
XM_005255955.5:c.578_589delinsTCAACCTACGCA	XP_005256012.1:p.Leu193=
XM_011523085.3:c.578_589delinsTCAACCTACGCA	XP_011521387.1:p.Leu193=
NR_163480.1:n.733+2566_733+2577delinsTCAACCTACGCA
NR_163481.1:n.577+2566_577+2577delinsTCAACCTACGCA