Canonical Allele Identifier: CA378072998
Gene: COL17A1 HGNC NCBI

Linked Data

gnomAD v4: 10-104057071-G-A
MyVariant Identifiers: chr10:g.105816829G>A (hg19) chr10:g.104057071G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104057071G>A , CM000672.2:g.104057071G>A GRCh38
NC_000010.10:g.105816829G>A , CM000672.1:g.105816829G>A GRCh37
NC_000010.9:g.105806819G>A NCBI36
NG_007069.1:g.33810C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.1369C>T ENSP00000358748.3:p.Pro457Ser
ENST00000648076.2:c.1369C>T MANE Select ENSP00000497653.1:p.Pro457Ser
ENST00000650263.1:c.1321C>T ENSP00000497850.1:p.Pro441Ser
ENST00000353479.9:c.1369C>T ENSP00000340937.5:p.Pro457Ser
ENST00000369733.7:c.1369C>T ENSP00000358748.3:p.Pro457Ser
NM_000494.3:c.1369C>T NP_000485.3:p.Pro457Ser
NM_000494.4:c.1369C>T MANE Select NP_000485.3:p.Pro457Ser
Search 100 bp 5'
Search 100 bp 3'