Canonical Allele Identifier: CA1933418716
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034620C= , CM000672.2:g.104034620C= GRCh38
NC_000010.10:g.105794378C= , CM000672.1:g.105794378C= GRCh37
NC_000010.9:g.105784368C= NCBI36
NG_007069.1:g.56261G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.3520+1G= ENSP00000358748.3:n.3520+1G=
ENST00000648076.2:c.3766+1G= MANE Select ENSP00000497653.1:n.3766+1G=
ENST00000353479.9:c.3766+1G= ENSP00000340937.5:n.3766+1G=
ENST00000369733.7:c.3520+1G= ENSP00000358748.3:n.3520+1G=
NM_000494.3:c.3766+1G= NP_000485.3:n.3766+1G=
NM_000494.4:c.3766+1G= MANE Select NP_000485.3:n.3766+1G=