Canonical Allele Identifier: CA2565414752
Gene: CHST3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008205_72008206insAC , CM000672.2:g.72008205_72008206insAC GRCh38
NC_000010.10:g.73767963_73767964insAC , CM000672.1:g.73767963_73767964insAC GRCh37
NC_000010.9:g.73437969_73437970insAC NCBI36
NG_012635.1:g.48844_48845insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1174_1175insAC MANE Select ENSP00000362207.4:p.Pro392HisfsTer3
ENST00000373115.4:c.1174_1175insAC ENSP00000362207.4:p.Pro392HisfsTer3
NM_004273.4:c.1174_1175insAC NP_004264.2:p.Pro392HisfsTer3
XM_006718075.2:c.1174_1175insAC XP_006718138.1:p.Pro392HisfsTer3
XM_011540369.1:c.1174_1175insAC XP_011538671.1:p.Pro392HisfsTer3
XM_006718075.4:c.1174_1175insAC XP_006718138.1:p.Pro392HisfsTer3
XM_011540369.2:c.1174_1175insAC XP_011538671.1:p.Pro392HisfsTer3
NM_004273.5:c.1174_1175insAC MANE Select NP_004264.2:p.Pro392HisfsTer3
Search 100 bp 5'
Search 100 bp 3'