Canonical Allele Identifier: CA2739276001
Gene: COL17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2826016
ClinVar RCV Id: RCV003681213

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104064529_104064744del , CM000672.2:g.104064529_104064744del GRCh38
NC_000010.10:g.105824287_105824502del , CM000672.1:g.105824287_105824502del GRCh37
NC_000010.9:g.105814277_105814492del NCBI36
NG_007069.1:g.26140_26355del

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.608-145_678del
ENST00000648076.2:c.608-145_678del
ENST00000649118.1:n.723-145_793del
ENST00000650263.1:c.560-145_630del
ENST00000353479.9:c.608-145_678del
ENST00000369733.7:c.608-145_678del
ENST00000393211.3:c.608-145_678del
NM_000494.3:c.608-145_678del
NM_000494.4:c.608-145_678del