Canonical Allele Identifier: CA5677808
Gene: COL17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2722870
ClinVar RCV Id: RCV003559121
dbSNP Id: rs181559014
ExAC: 10:105794082 C / T
gnomAD v2: 10-105794082-C-T
gnomAD v3: 10-104034324-C-T
gnomAD v4: 10-104034324-C-T
MyVariant Identifiers: chr10:g.105794082C>T (hg19) chr10:g.104034324C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034324C>T , CM000672.2:g.104034324C>T GRCh38
NC_000010.10:g.105794082C>T , CM000672.1:g.105794082C>T GRCh37
NC_000010.9:g.105784072C>T NCBI36
NG_007069.1:g.56557G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.3531G>A ENSP00000358748.3:p.Val1177=
ENST00000648076.2:c.3777G>A MANE Select ENSP00000497653.1:p.Val1259=
ENST00000353479.9:c.3777G>A ENSP00000340937.5:p.Val1259=
ENST00000369733.7:c.3531G>A ENSP00000358748.3:p.Val1177=
NM_000494.3:c.3777G>A NP_000485.3:p.Val1259=
NM_000494.4:c.3777G>A MANE Select NP_000485.3:p.Val1259=
Search 100 bp 5'
Search 100 bp 3'