Canonical Allele Identifier: CA1933389896
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104038310_104038312delinsCTT , CM000672.2:g.104038310_104038312delinsCTT GRCh38
NC_000010.10:g.105798068_105798070delinsCTT , CM000672.1:g.105798068_105798070delinsCTT GRCh37
NC_000010.9:g.105788058_105788060delinsCTT NCBI36
NG_007069.1:g.52569_52571delinsAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.2935+94_2935+96delinsAAG ENSP00000358748.3:n.2935+94_2935+96delins...
ENST00000648076.2:c.3070+94_3070+96delinsAAG MANE Select ENSP00000497653.1:n.3070+94_3070+96delins...
ENST00000353479.9:c.3070+94_3070+96delinsAAG ENSP00000340937.5:n.3070+94_3070+96delins...
ENST00000369733.7:c.2935+94_2935+96delinsAAG ENSP00000358748.3:n.2935+94_2935+96delins...
NM_000494.3:c.3070+94_3070+96delinsAAG NP_000485.3:n.3070+94_3070+96delinsAAG
NM_000494.4:c.3070+94_3070+96delinsAAG MANE Select NP_000485.3:n.3070+94_3070+96delinsAAG