Canonical Allele Identifier: CA2695212418
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008114_72008121delinsCGGCA , CM000672.2:g.72008114_72008121delinsCGGCA GRCh38
NC_000010.10:g.73767872_73767879delinsCGGCA , CM000672.1:g.73767872_73767879delinsCGGCA GRCh37
NC_000010.9:g.73437878_73437885delinsCGGCA NCBI36
NG_012635.1:g.48753_48760delinsCGGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1083_1090delinsCGGCA MANE Select ENSP00000362207.4:p.Trp361_Gly364delinsCysGlySer
ENST00000373115.4:c.1083_1090delinsCGGCA ENSP00000362207.4:p.Trp361_Gly364delinsCysGlySer
NM_004273.4:c.1083_1090delinsCGGCA NP_004264.2:p.Trp361_Gly364delinsCysGlySer
XM_006718075.2:c.1083_1090delinsCGGCA XP_006718138.1:p.Trp361_Gly364delinsCysGlySer
XM_011540369.1:c.1083_1090delinsCGGCA XP_011538671.1:p.Trp361_Gly364delinsCysGlySer
XM_006718075.4:c.1083_1090delinsCGGCA XP_006718138.1:p.Trp361_Gly364delinsCysGlySer
XM_011540369.2:c.1083_1090delinsCGGCA XP_011538671.1:p.Trp361_Gly364delinsCysGlySer
NM_004273.5:c.1083_1090delinsCGGCA MANE Select NP_004264.2:p.Trp361_Gly364delinsCysGlySer