Canonical Allele Identifier: CA471341980
Gene: COL17A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.105794470A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034712A>T , CM000672.2:g.104034712A>T GRCh38
NC_000010.10:g.105794470A>T , CM000672.1:g.105794470A>T GRCh37
NC_000010.9:g.105784460A>T NCBI36
NG_007069.1:g.56169T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.3429T>A ENSP00000358748.3:p.Pro1143=
ENST00000648076.2:c.3675T>A MANE Select ENSP00000497653.1:p.Pro1225=
ENST00000353479.9:c.3675T>A ENSP00000340937.5:p.Pro1225=
ENST00000369733.7:c.3429T>A ENSP00000358748.3:p.Pro1143=
NM_000494.3:c.3675T>A NP_000485.3:p.Pro1225=
NM_000494.4:c.3675T>A MANE Select NP_000485.3:p.Pro1225=
Search 100 bp 5'
Search 100 bp 3'