Canonical Allele Identifier: CA378077115

Gene: COL17A1

Linked Data

• MyVariant Identifiers: chr10:g.105824194A>T (hg19) ; chr10:g.104064436A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104064436A>T , CM000672.2:g.104064436A>T	GRCh38
NC_000010.10:g.105824194A>T , CM000672.1:g.105824194A>T	GRCh37
NC_000010.9:g.105814184A>T	NCBI36
NG_007069.1:g.26445T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369733.8:c.766+2T>A	ENSP00000358748.3:n.766+2T>A
ENST00000648076.2:c.766+2T>A MANE Select	ENSP00000497653.1:n.766+2T>A
ENST00000649118.1:n.881+2T>A
ENST00000650263.1:c.718+2T>A	ENSP00000497850.1:n.718+2T>A
ENST00000353479.9:c.766+2T>A	ENSP00000340937.5:n.766+2T>A
ENST00000369733.7:c.766+2T>A	ENSP00000358748.3:n.766+2T>A
ENST00000393211.3:c.766+2T>A	ENSP00000376905.3:n.766+2T>A
ENST00000488320.1:n.111+2T>A
NM_000494.3:c.766+2T>A	NP_000485.3:n.766+2T>A
NM_000494.4:c.766+2T>A MANE Select	NP_000485.3:n.766+2T>A