Canonical Allele Identifier: CA1933418665
Gene: COL17A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034528C= , CM000672.2:g.104034528C= GRCh38
NC_000010.10:g.105794286C= , CM000672.1:g.105794286C= GRCh37
NC_000010.9:g.105784276C= NCBI36
NG_007069.1:g.56353G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.3520+93G= ENSP00000358748.3:n.3520+93G=
ENST00000648076.2:c.3766+93G= MANE Select ENSP00000497653.1:n.3766+93G=
ENST00000353479.9:c.3766+93G= ENSP00000340937.5:n.3766+93G=
ENST00000369733.7:c.3520+93G= ENSP00000358748.3:n.3520+93G=
NM_000494.3:c.3766+93G= NP_000485.3:n.3766+93G=
NM_000494.4:c.3766+93G= MANE Select NP_000485.3:n.3766+93G=
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