Canonical Allele Identifier: CA2610800294
Gene: COL17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104064588del , CM000672.2:g.104064588del GRCh38
NC_000010.10:g.105824346del , CM000672.1:g.105824346del GRCh37
NC_000010.9:g.105814336del NCBI36
NG_007069.1:g.26293del

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.616del ENSP00000358748.3:p.Thr206ProfsTer?
ENST00000648076.2:c.616del MANE Select ENSP00000497653.1:p.Thr206ProfsTer?
ENST00000649118.1:n.731del
ENST00000650263.1:c.568del ENSP00000497850.1:p.Thr190ProfsTer?
ENST00000353479.9:c.616del ENSP00000340937.5:p.Thr206ProfsTer?
ENST00000369733.7:c.616del ENSP00000358748.3:p.Thr206ProfsTer?
ENST00000393211.3:c.616del ENSP00000376905.3:p.Thr206ProfsTer?
NM_000494.3:c.616del NP_000485.3:p.Thr206ProfsTer?
NM_000494.4:c.616del MANE Select NP_000485.3:p.Thr206ProfsTer?