Canonical Allele Identifier: CA1918976735
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1840065056
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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
Search 100 bp 5'
Search 100 bp 3'