Canonical Allele Identifier: CA378079969
Gene: COL17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104072073T>C , CM000672.2:g.104072073T>C GRCh38
NC_000010.10:g.105831831T>C , CM000672.1:g.105831831T>C GRCh37
NC_000010.9:g.105821821T>C NCBI36
NG_007069.1:g.18808A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.422A>G ENSP00000358748.3:p.Glu141Gly
ENST00000648076.2:c.422A>G MANE Select ENSP00000497653.1:p.Glu141Gly
ENST00000649118.1:n.537A>G
ENST00000650263.1:c.374A>G ENSP00000497850.1:p.Glu125Gly
ENST00000353479.9:c.422A>G ENSP00000340937.5:p.Glu141Gly
ENST00000369733.7:c.422A>G ENSP00000358748.3:p.Glu141Gly
ENST00000393211.3:c.422A>G ENSP00000376905.3:p.Glu141Gly
ENST00000483876.1:n.472A>G
NM_000494.3:c.422A>G NP_000485.3:p.Glu141Gly
NM_000494.4:c.422A>G MANE Select NP_000485.3:p.Glu141Gly