Canonical Allele Identifier: CA1933389825
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104038225C= , CM000672.2:g.104038225C= GRCh38
NC_000010.10:g.105797983C= , CM000672.1:g.105797983C= GRCh37
NC_000010.9:g.105787973C= NCBI36
NG_007069.1:g.52656G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.2935+181G= ENSP00000358748.3:n.2935+181G=
ENST00000648076.2:c.3070+181G= MANE Select ENSP00000497653.1:n.3070+181G=
ENST00000353479.9:c.3070+181G= ENSP00000340937.5:n.3070+181G=
ENST00000369733.7:c.2935+181G= ENSP00000358748.3:n.2935+181G=
NM_000494.3:c.3070+181G= NP_000485.3:n.3070+181G=
NM_000494.4:c.3070+181G= MANE Select NP_000485.3:n.3070+181G=