Canonical Allele Identifier: CA5548224
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs767987808
ExAC: 10:73768048 ACTC / A
gnomAD v2: 10-73768048-ACTC-A
gnomAD v3: 10-72008290-ACTC-A
gnomAD v4: 10-72008290-ACTC-A
MyVariant Identifiers: chr10:g.73768049_73768051del (hg19) chr10:g.72008291_72008293del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008294_72008296del , CM000672.2:g.72008294_72008296del GRCh38
NC_000010.10:g.73768052_73768054del , CM000672.1:g.73768052_73768054del GRCh37
NC_000010.9:g.73438058_73438060del NCBI36
NG_012635.1:g.48933_48935del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1263_1265del MANE Select ENSP00000362207.4:p.Ser422del
ENST00000373115.4:c.1263_1265del ENSP00000362207.4:p.Ser422del
NM_004273.4:c.1263_1265del NP_004264.2:p.Ser422del
XM_006718075.2:c.1263_1265del XP_006718138.1:p.Ser422del
XM_011540369.1:c.1263_1265del XP_011538671.1:p.Ser422del
XM_006718075.4:c.1263_1265del XP_006718138.1:p.Ser422del
XM_011540369.2:c.1263_1265del XP_011538671.1:p.Ser422del
NM_004273.5:c.1263_1265del MANE Select NP_004264.2:p.Ser422del
Search 100 bp 5'
Search 100 bp 3'