Canonical Allele Identifier: CA5677767
Gene: COL17A1 HGNC NCBI

Linked Data

dbSNP Id: rs752418541

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034205G>A , CM000672.2:g.104034205G>A GRCh38
NC_000010.10:g.105793963G>A , CM000672.1:g.105793963G>A GRCh37
NC_000010.9:g.105783953G>A NCBI36
NG_007069.1:g.56676C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.3650C>T ENSP00000358748.3:p.Ser1217Leu
ENST00000648076.2:c.3896C>T MANE Select ENSP00000497653.1:p.Ser1299Leu
ENST00000353479.9:c.3896C>T ENSP00000340937.5:p.Ser1299Leu
ENST00000369733.7:c.3650C>T ENSP00000358748.3:p.Ser1217Leu
NM_000494.3:c.3896C>T NP_000485.3:p.Ser1299Leu
NM_000494.4:c.3896C>T MANE Select NP_000485.3:p.Ser1299Leu