Canonical Allele Identifier: CA378079942
Gene: COL17A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104072070A>G , CM000672.2:g.104072070A>G GRCh38
NC_000010.10:g.105831828A>G , CM000672.1:g.105831828A>G GRCh37
NC_000010.9:g.105821818A>G NCBI36
NG_007069.1:g.18811T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.425T>C ENSP00000358748.3:p.Ile142Thr
ENST00000648076.2:c.425T>C MANE Select ENSP00000497653.1:p.Ile142Thr
ENST00000649118.1:n.540T>C
ENST00000650263.1:c.377T>C ENSP00000497850.1:p.Ile126Thr
ENST00000353479.9:c.425T>C ENSP00000340937.5:p.Ile142Thr
ENST00000369733.7:c.425T>C ENSP00000358748.3:p.Ile142Thr
ENST00000393211.3:c.425T>C ENSP00000376905.3:p.Ile142Thr
ENST00000483876.1:n.475T>C
NM_000494.3:c.425T>C NP_000485.3:p.Ile142Thr
NM_000494.4:c.425T>C MANE Select NP_000485.3:p.Ile142Thr