Canonical Allele Identifier: CA2610801261
Gene: COL17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104038327G>A , CM000672.2:g.104038327G>A GRCh38
NC_000010.10:g.105798085G>A , CM000672.1:g.105798085G>A GRCh37
NC_000010.9:g.105788075G>A NCBI36
NG_007069.1:g.52554C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.2935+79C>T ENSP00000358748.3:n.2935+79C>T
ENST00000648076.2:c.3070+79C>T MANE Select ENSP00000497653.1:n.3070+79C>T
ENST00000353479.9:c.3070+79C>T ENSP00000340937.5:n.3070+79C>T
ENST00000369733.7:c.2935+79C>T ENSP00000358748.3:n.2935+79C>T
NM_000494.3:c.3070+79C>T NP_000485.3:n.3070+79C>T
NM_000494.4:c.3070+79C>T MANE Select NP_000485.3:n.3070+79C>T