Canonical Allele Identifier: CA378077651
Gene: COL17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104064576T>A , CM000672.2:g.104064576T>A GRCh38
NC_000010.10:g.105824334T>A , CM000672.1:g.105824334T>A GRCh37
NC_000010.9:g.105814324T>A NCBI36
NG_007069.1:g.26305A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.628A>T ENSP00000358748.3:p.Thr210Ser
ENST00000648076.2:c.628A>T MANE Select ENSP00000497653.1:p.Thr210Ser
ENST00000649118.1:n.743A>T
ENST00000650263.1:c.580A>T ENSP00000497850.1:p.Thr194Ser
ENST00000353479.9:c.628A>T ENSP00000340937.5:p.Thr210Ser
ENST00000369733.7:c.628A>T ENSP00000358748.3:p.Thr210Ser
ENST00000393211.3:c.628A>T ENSP00000376905.3:p.Thr210Ser
NM_000494.3:c.628A>T NP_000485.3:p.Thr210Ser
NM_000494.4:c.628A>T MANE Select NP_000485.3:p.Thr210Ser