Canonical Allele Identifier: CA378077725

Gene: COL17A1

Linked Data

• MyVariant Identifiers: chr10:g.105824348C>A (hg19) ; chr10:g.104064590C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104064590C>A , CM000672.2:g.104064590C>A	GRCh38
NC_000010.10:g.105824348C>A , CM000672.1:g.105824348C>A	GRCh37
NC_000010.9:g.105814338C>A	NCBI36
NG_007069.1:g.26291G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369733.8:c.614G>T	ENSP00000358748.3:p.Gly205Val
ENST00000648076.2:c.614G>T MANE Select	ENSP00000497653.1:p.Gly205Val
ENST00000649118.1:n.729G>T
ENST00000650263.1:c.566G>T	ENSP00000497850.1:p.Gly189Val
ENST00000353479.9:c.614G>T	ENSP00000340937.5:p.Gly205Val
ENST00000369733.7:c.614G>T	ENSP00000358748.3:p.Gly205Val
ENST00000393211.3:c.614G>T	ENSP00000376905.3:p.Gly205Val
NM_000494.3:c.614G>T	NP_000485.3:p.Gly205Val
NM_000494.4:c.614G>T MANE Select	NP_000485.3:p.Gly205Val