Canonical Allele Identifier: CA378077710
Gene: COL17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104064587G>C , CM000672.2:g.104064587G>C GRCh38
NC_000010.10:g.105824345G>C , CM000672.1:g.105824345G>C GRCh37
NC_000010.9:g.105814335G>C NCBI36
NG_007069.1:g.26294C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.617C>G ENSP00000358748.3:p.Thr206Ser
ENST00000648076.2:c.617C>G MANE Select ENSP00000497653.1:p.Thr206Ser
ENST00000649118.1:n.732C>G
ENST00000650263.1:c.569C>G ENSP00000497850.1:p.Thr190Ser
ENST00000353479.9:c.617C>G ENSP00000340937.5:p.Thr206Ser
ENST00000369733.7:c.617C>G ENSP00000358748.3:p.Thr206Ser
ENST00000393211.3:c.617C>G ENSP00000376905.3:p.Thr206Ser
NM_000494.3:c.617C>G NP_000485.3:p.Thr206Ser
NM_000494.4:c.617C>G MANE Select NP_000485.3:p.Thr206Ser