Canonical Allele Identifier: CA471338926

Gene: COL17A1

Linked Data

• gnomAD v4: 10-104064595-C-A
• MyVariant Identifiers: chr10:g.105824353C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104064595C>A , CM000672.2:g.104064595C>A	GRCh38
NC_000010.10:g.105824353C>A , CM000672.1:g.105824353C>A	GRCh37
NC_000010.9:g.105814343C>A	NCBI36
NG_007069.1:g.26286G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369733.8:c.609G>T	ENSP00000358748.3:p.Val203=
ENST00000648076.2:c.609G>T MANE Select	ENSP00000497653.1:p.Val203=
ENST00000649118.1:n.724G>T
ENST00000650263.1:c.561G>T	ENSP00000497850.1:p.Val187=
ENST00000353479.9:c.609G>T	ENSP00000340937.5:p.Val203=
ENST00000369733.7:c.609G>T	ENSP00000358748.3:p.Val203=
ENST00000393211.3:c.609G>T	ENSP00000376905.3:p.Val203=
NM_000494.3:c.609G>T	NP_000485.3:p.Val203=
NM_000494.4:c.609G>T MANE Select	NP_000485.3:p.Val203=