Canonical Allele Identifier: CA378079985
Gene: COL17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104072075A>T , CM000672.2:g.104072075A>T GRCh38
NC_000010.10:g.105831833A>T , CM000672.1:g.105831833A>T GRCh37
NC_000010.9:g.105821823A>T NCBI36
NG_007069.1:g.18806T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.420T>A ENSP00000358748.3:p.Ser140Arg
ENST00000648076.2:c.420T>A MANE Select ENSP00000497653.1:p.Ser140Arg
ENST00000649118.1:n.535T>A
ENST00000650263.1:c.372T>A ENSP00000497850.1:p.Ser124Arg
ENST00000353479.9:c.420T>A ENSP00000340937.5:p.Ser140Arg
ENST00000369733.7:c.420T>A ENSP00000358748.3:p.Ser140Arg
ENST00000393211.3:c.420T>A ENSP00000376905.3:p.Ser140Arg
ENST00000483876.1:n.470T>A
NM_000494.3:c.420T>A NP_000485.3:p.Ser140Arg
NM_000494.4:c.420T>A MANE Select NP_000485.3:p.Ser140Arg