Canonical Allele Identifier: CA1933418346
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034200_104034204delinsCAGAT , CM000672.2:g.104034200_104034204delinsCAGAT GRCh38
NC_000010.10:g.105793958_105793962delinsCAGAT , CM000672.1:g.105793958_105793962delinsCAGAT GRCh37
NC_000010.9:g.105783948_105783952delinsCAGAT NCBI36
NG_007069.1:g.56677_56681delinsATCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.3651_3655delinsATCTG ENSP00000358748.3:p.Ser1217=
ENST00000648076.2:c.3897_3901delinsATCTG MANE Select ENSP00000497653.1:p.Ser1299=
ENST00000353479.9:c.3897_3901delinsATCTG ENSP00000340937.5:p.Ser1299=
ENST00000369733.7:c.3651_3655delinsATCTG ENSP00000358748.3:p.Ser1217=
NM_000494.3:c.3897_3901delinsATCTG NP_000485.3:p.Ser1299=
NM_000494.4:c.3897_3901delinsATCTG MANE Select NP_000485.3:p.Ser1299=