Canonical Allele Identifier: CA378077646
Gene: COL17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104064575G>T , CM000672.2:g.104064575G>T GRCh38
NC_000010.10:g.105824333G>T , CM000672.1:g.105824333G>T GRCh37
NC_000010.9:g.105814323G>T NCBI36
NG_007069.1:g.26306C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.629C>A ENSP00000358748.3:p.Thr210Lys
ENST00000648076.2:c.629C>A MANE Select ENSP00000497653.1:p.Thr210Lys
ENST00000649118.1:n.744C>A
ENST00000650263.1:c.581C>A ENSP00000497850.1:p.Thr194Lys
ENST00000353479.9:c.629C>A ENSP00000340937.5:p.Thr210Lys
ENST00000369733.7:c.629C>A ENSP00000358748.3:p.Thr210Lys
ENST00000393211.3:c.629C>A ENSP00000376905.3:p.Thr210Lys
NM_000494.3:c.629C>A NP_000485.3:p.Thr210Lys
NM_000494.4:c.629C>A MANE Select NP_000485.3:p.Thr210Lys