Canonical Allele Identifier: CA1933389814
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104038223_104038243delinsGACACACATACACACACACAC , CM000672.2:g.104038223_104038243delinsGACACACATACACACACACAC GRCh38
NC_000010.10:g.105797981_105798001delinsGACACACATACACACACACAC , CM000672.1:g.105797981_105798001delinsGACACACATACACACACACAC GRCh37
NC_000010.9:g.105787971_105787991delinsGACACACATACACACACACAC NCBI36
NG_007069.1:g.52638_52658delinsGTGTGTGTGTGTATGTGTGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.2935+163_2935+183delinsGTGTGTGTGTGTATGTGTGTC ENSP00000358748.3:n.2935+163_2935+183delinsGTGTGTGTGTGTATGTGT...
ENST00000648076.2:c.3070+163_3070+183delinsGTGTGTGTGTGTATGTGTGTC MANE Select ENSP00000497653.1:n.3070+163_3070+183delinsGTGTGTGTGTGTATGTGT...
ENST00000353479.9:c.3070+163_3070+183delinsGTGTGTGTGTGTATGTGTGTC ENSP00000340937.5:n.3070+163_3070+183delinsGTGTGTGTGTGTATGTGT...
ENST00000369733.7:c.2935+163_2935+183delinsGTGTGTGTGTGTATGTGTGTC ENSP00000358748.3:n.2935+163_2935+183delinsGTGTGTGTGTGTATGTGT...
NM_000494.3:c.3070+163_3070+183delinsGTGTGTGTGTGTATGTGTGTC NP_000485.3:n.3070+163_3070+183delinsGTGTGTGTGTGTATGTGTGTC
NM_000494.4:c.3070+163_3070+183delinsGTGTGTGTGTGTATGTGTGTC MANE Select NP_000485.3:n.3070+163_3070+183delinsGTGTGTGTGTGTATGTGTGTC