Canonical Allele Identifier: CA378067155
Gene: COL17A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.105797432T>G (hg19) chr10:g.104037674T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104037674T>G , CM000672.2:g.104037674T>G GRCh38
NC_000010.10:g.105797432T>G , CM000672.1:g.105797432T>G GRCh37
NC_000010.9:g.105787422T>G NCBI36
NG_007069.1:g.53207A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.3035A>C ENSP00000358748.3:p.Tyr1012Ser
ENST00000648076.2:c.3170A>C MANE Select ENSP00000497653.1:p.Tyr1057Ser
ENST00000353479.9:c.3170A>C ENSP00000340937.5:p.Tyr1057Ser
ENST00000369733.7:c.3035A>C ENSP00000358748.3:p.Tyr1012Ser
NM_000494.3:c.3170A>C NP_000485.3:p.Tyr1057Ser
NM_000494.4:c.3170A>C MANE Select NP_000485.3:p.Tyr1057Ser
Search 100 bp 5'
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