Canonical Allele Identifier: CA1933418532
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034314T= , CM000672.2:g.104034314T= GRCh38
NC_000010.10:g.105794072T= , CM000672.1:g.105794072T= GRCh37
NC_000010.9:g.105784062T= NCBI36
NG_007069.1:g.56567A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.3541A= ENSP00000358748.3:p.Ile1181=
ENST00000648076.2:c.3787A= MANE Select ENSP00000497653.1:p.Ile1263=
ENST00000353479.9:c.3787A= ENSP00000340937.5:p.Ile1263=
ENST00000369733.7:c.3541A= ENSP00000358748.3:p.Ile1181=
NM_000494.3:c.3787A= NP_000485.3:p.Ile1263=
NM_000494.4:c.3787A= MANE Select NP_000485.3:p.Ile1263=