Canonical Allele Identifier: CA471338896
Gene: COL17A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.105824338A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104064580A>G , CM000672.2:g.104064580A>G GRCh38
NC_000010.10:g.105824338A>G , CM000672.1:g.105824338A>G GRCh37
NC_000010.9:g.105814328A>G NCBI36
NG_007069.1:g.26301T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.624T>C ENSP00000358748.3:p.Asp208=
ENST00000648076.2:c.624T>C MANE Select ENSP00000497653.1:p.Asp208=
ENST00000649118.1:n.739T>C
ENST00000650263.1:c.576T>C ENSP00000497850.1:p.Asp192=
ENST00000353479.9:c.624T>C ENSP00000340937.5:p.Asp208=
ENST00000369733.7:c.624T>C ENSP00000358748.3:p.Asp208=
ENST00000393211.3:c.624T>C ENSP00000376905.3:p.Asp208=
NM_000494.3:c.624T>C NP_000485.3:p.Asp208=
NM_000494.4:c.624T>C MANE Select NP_000485.3:p.Asp208=