Canonical Allele Identifier: CA2610796349
Gene: COL17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-104033911-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104033911C>T , CM000672.2:g.104033911C>T GRCh38
NC_000010.10:g.105793669C>T , CM000672.1:g.105793669C>T GRCh37
NC_000010.9:g.105783659C>T NCBI36
NG_007069.1:g.56970G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.3910+34G>A ENSP00000358748.3:n.3910+34G>A
ENST00000647647.1:c.186+34G>A
ENST00000648076.2:c.4156+34G>A MANE Select ENSP00000497653.1:n.4156+34G>A
ENST00000353479.9:c.4156+34G>A ENSP00000340937.5:n.4156+34G>A
ENST00000369733.7:c.3910+34G>A ENSP00000358748.3:n.3910+34G>A
NM_000494.3:c.4156+34G>A NP_000485.3:n.4156+34G>A
NM_000494.4:c.4156+34G>A MANE Select NP_000485.3:n.4156+34G>A
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