Canonical Allele Identifier: CA471344752
Gene: COL17A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.105798177A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104038419A>G , CM000672.2:g.104038419A>G GRCh38
NC_000010.10:g.105798177A>G , CM000672.1:g.105798177A>G GRCh37
NC_000010.9:g.105788167A>G NCBI36
NG_007069.1:g.52462T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.2922T>C ENSP00000358748.3:p.Ser974=
ENST00000648076.2:c.3057T>C MANE Select ENSP00000497653.1:p.Ser1019=
ENST00000353479.9:c.3057T>C ENSP00000340937.5:p.Ser1019=
ENST00000369733.7:c.2922T>C ENSP00000358748.3:p.Ser974=
NM_000494.3:c.3057T>C NP_000485.3:p.Ser1019=
NM_000494.4:c.3057T>C MANE Select NP_000485.3:p.Ser1019=