Canonical Allele Identifier: CA378067102
Gene: COL17A1 HGNC NCBI

Linked Data

dbSNP Id: rs2086313785
gnomAD v3: 10-104037650-A-C
gnomAD v4: 10-104037650-A-C
MyVariant Identifiers: chr10:g.105797408A>C (hg19) chr10:g.104037650A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104037650A>C , CM000672.2:g.104037650A>C GRCh38
NC_000010.10:g.105797408A>C , CM000672.1:g.105797408A>C GRCh37
NC_000010.9:g.105787398A>C NCBI36
NG_007069.1:g.53231T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.3059T>G ENSP00000358748.3:p.Val1020Gly
ENST00000648076.2:c.3194T>G MANE Select ENSP00000497653.1:p.Val1065Gly
ENST00000353479.9:c.3194T>G ENSP00000340937.5:p.Val1065Gly
ENST00000369733.7:c.3059T>G ENSP00000358748.3:p.Val1020Gly
NM_000494.3:c.3194T>G NP_000485.3:p.Val1065Gly
NM_000494.4:c.3194T>G MANE Select NP_000485.3:p.Val1065Gly
Search 100 bp 5'
Search 100 bp 3'