Canonical Allele Identifier: CA1933389835
Gene: COL17A1 HGNC NCBI

Linked Data

dbSNP Id: rs2086321289

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104038232_104038248del , CM000672.2:g.104038232_104038248del GRCh38
NC_000010.10:g.105797990_105798006del , CM000672.1:g.105797990_105798006del GRCh37
NC_000010.9:g.105787980_105787996del NCBI36
NG_007069.1:g.52633_52649del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.2935+158_2935+174del ENSP00000358748.3:n.2935+158_2935+174del
ENST00000648076.2:c.3070+158_3070+174del MANE Select ENSP00000497653.1:n.3070+158_3070+174del
ENST00000353479.9:c.3070+158_3070+174del ENSP00000340937.5:n.3070+158_3070+174del
ENST00000369733.7:c.2935+158_2935+174del ENSP00000358748.3:n.2935+158_2935+174del
NM_000494.3:c.3070+158_3070+174del NP_000485.3:n.3070+158_3070+174del
NM_000494.4:c.3070+158_3070+174del MANE Select NP_000485.3:n.3070+158_3070+174del