Canonical Allele Identifier: CA2788492448

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72010028_72010029insAAAAAA , CM000672.2:g.72010028_72010029insAAAAAA	GRCh38
NC_000010.10:g.73769786_73769787insAAAAAA , CM000672.1:g.73769786_73769787insAAAAAA	GRCh37
NC_000010.9:g.73439792_73439793insAAAAAA	NCBI36
NG_012635.1:g.50667_50668insAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1557_*1558insAAAAAA MANE Select	ENSP00000362207.4:n.*1557_*1558insAAAAAA
ENST00000373115.4:c.*1557_*1558insAAAAAA	ENSP00000362207.4:n.*1557_*1558insAAAAAA
NM_004273.4:c.*1557_*1558insAAAAAA	NP_004264.2:n.*1557_*1558insAAAAAA
XM_006718075.2:c.*1557_*1558insAAAAAA	XP_006718138.1:n.*1557_*1558insAAAAAA
XM_011540369.1:c.*1557_*1558insAAAAAA	XP_011538671.1:n.*1557_*1558insAAAAAA
XM_006718075.4:c.*1557_*1558insAAAAAA	XP_006718138.1:n.*1557_*1558insAAAAAA
XM_011540369.2:c.*1557_*1558insAAAAAA	XP_011538671.1:n.*1557_*1558insAAAAAA
NM_004273.5:c.*1557_*1558insAAAAAA MANE Select	NP_004264.2:n.*1557_*1558insAAAAAA