Canonical Allele Identifier: CA1933403181
Gene: COL17A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104053202C= , CM000672.2:g.104053202C= GRCh38
NC_000010.10:g.105812960C= , CM000672.1:g.105812960C= GRCh37
NC_000010.9:g.105802950C= NCBI36
NG_007069.1:g.37679G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.1835-67G= ENSP00000358748.3:n.1835-67G=
ENST00000648076.2:c.1835-67G= MANE Select ENSP00000497653.1:n.1835-67G=
ENST00000650263.1:c.1787-67G= ENSP00000497850.1:n.1787-67G=
ENST00000353479.9:c.1835-67G= ENSP00000340937.5:n.1835-67G=
ENST00000369733.7:c.1835-67G= ENSP00000358748.3:n.1835-67G=
NM_000494.3:c.1835-67G= NP_000485.3:n.1835-67G=
NM_000494.4:c.1835-67G= MANE Select NP_000485.3:n.1835-67G=
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