Canonical Allele Identifier: CA378067379
Gene: COL17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104038409G>T , CM000672.2:g.104038409G>T GRCh38
NC_000010.10:g.105798167G>T , CM000672.1:g.105798167G>T GRCh37
NC_000010.9:g.105788157G>T NCBI36
NG_007069.1:g.52472C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.2932C>A ENSP00000358748.3:p.Gln978Lys
ENST00000648076.2:c.3067C>A MANE Select ENSP00000497653.1:p.Gln1023Lys
ENST00000353479.9:c.3067C>A ENSP00000340937.5:p.Gln1023Lys
ENST00000369733.7:c.2932C>A ENSP00000358748.3:p.Gln978Lys
NM_000494.3:c.3067C>A NP_000485.3:p.Gln1023Lys
NM_000494.4:c.3067C>A MANE Select NP_000485.3:p.Gln1023Lys