Canonical Allele Identifier: CA1933418338
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034196C= , CM000672.2:g.104034196C= GRCh38
NC_000010.10:g.105793954C= , CM000672.1:g.105793954C= GRCh37
NC_000010.9:g.105783944C= NCBI36
NG_007069.1:g.56685G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.3659G= ENSP00000358748.3:p.Arg1220=
ENST00000648076.2:c.3905G= MANE Select ENSP00000497653.1:p.Arg1302=
ENST00000353479.9:c.3905G= ENSP00000340937.5:p.Arg1302=
ENST00000369733.7:c.3659G= ENSP00000358748.3:p.Arg1220=
NM_000494.3:c.3905G= NP_000485.3:p.Arg1302=
NM_000494.4:c.3905G= MANE Select NP_000485.3:p.Arg1302=