Canonical Allele Identifier: CA378079975
Gene: COL17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104072074C>A , CM000672.2:g.104072074C>A GRCh38
NC_000010.10:g.105831832C>A , CM000672.1:g.105831832C>A GRCh37
NC_000010.9:g.105821822C>A NCBI36
NG_007069.1:g.18807G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.421G>T ENSP00000358748.3:p.Glu141Ter
ENST00000648076.2:c.421G>T MANE Select ENSP00000497653.1:p.Glu141Ter
ENST00000649118.1:n.536G>T
ENST00000650263.1:c.373G>T ENSP00000497850.1:p.Glu125Ter
ENST00000353479.9:c.421G>T ENSP00000340937.5:p.Glu141Ter
ENST00000369733.7:c.421G>T ENSP00000358748.3:p.Glu141Ter
ENST00000393211.3:c.421G>T ENSP00000376905.3:p.Glu141Ter
ENST00000483876.1:n.471G>T
NM_000494.3:c.421G>T NP_000485.3:p.Glu141Ter
NM_000494.4:c.421G>T MANE Select NP_000485.3:p.Glu141Ter