Canonical Allele Identifier: CA1918976735

Gene: CHST3

Linked Data

• dbSNP Id: rs1840065056

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72008103_72008120del , CM000672.2:g.72008103_72008120del	GRCh38
NC_000010.10:g.73767861_73767878del , CM000672.1:g.73767861_73767878del	GRCh37
NC_000010.9:g.73437867_73437884del	NCBI36
NG_012635.1:g.48742_48759del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.1072_1089del MANE Select	ENSP00000362207.4:p.Gln358_Arg363del
ENST00000373115.4:c.1072_1089del	ENSP00000362207.4:p.Gln358_Arg363del
NM_004273.4:c.1072_1089del	NP_004264.2:p.Gln358_Arg363del
XM_006718075.2:c.1072_1089del	XP_006718138.1:p.Gln358_Arg363del
XM_011540369.1:c.1072_1089del	XP_011538671.1:p.Gln358_Arg363del
XM_006718075.4:c.1072_1089del	XP_006718138.1:p.Gln358_Arg363del
XM_011540369.2:c.1072_1089del	XP_011538671.1:p.Gln358_Arg363del
NM_004273.5:c.1072_1089del MANE Select	NP_004264.2:p.Gln358_Arg363del