Canonical Allele Identifier: CA2610801269
Gene: COL17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104038329T>C , CM000672.2:g.104038329T>C GRCh38
NC_000010.10:g.105798087T>C , CM000672.1:g.105798087T>C GRCh37
NC_000010.9:g.105788077T>C NCBI36
NG_007069.1:g.52552A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.2935+77A>G ENSP00000358748.3:n.2935+77A>G
ENST00000648076.2:c.3070+77A>G MANE Select ENSP00000497653.1:n.3070+77A>G
ENST00000353479.9:c.3070+77A>G ENSP00000340937.5:n.3070+77A>G
ENST00000369733.7:c.2935+77A>G ENSP00000358748.3:n.2935+77A>G
NM_000494.3:c.3070+77A>G NP_000485.3:n.3070+77A>G
NM_000494.4:c.3070+77A>G MANE Select NP_000485.3:n.3070+77A>G