Canonical Allele Identifier: CA2697558776
Community Standard Title: NM_000494.4(COL17A1):c.911-12C>G
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104061485G>C , CM000672.2:g.104061485G>C GRCh38
NC_000010.10:g.105821243G>C , CM000672.1:g.105821243G>C GRCh37
NC_000010.9:g.105811233G>C NCBI36
NG_007069.1:g.29396C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000494.4:c.911-12C>G MANE Select NP_000485.3:n.911-12C>G
ENST00000648076.2:c.911-12C>G MANE Select ENSP00000497653.1:n.911-12C>G
NM_000494.3:c.911-12C>G NP_000485.3:n.911-12C>G
ENST00000353479.9:c.911-12C>G ENSP00000340937.5:n.911-12C>G
ENST00000369733.7:c.911-12C>G ENSP00000358748.3:n.911-12C>G
ENST00000369733.8:c.911-12C>G ENSP00000358748.3:n.911-12C>G
ENST00000393211.3:c.911-12C>G ENSP00000376905.3:n.911-12C>G
ENST00000488320.1:n.362-12C>G
ENST00000650263.1:c.863-12C>G ENSP00000497850.1:n.863-12C>G