Canonical Allele Identifier: CA1933418147
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034109G= , CM000672.2:g.104034109G= GRCh38
NC_000010.10:g.105793867G= , CM000672.1:g.105793867G= GRCh37
NC_000010.9:g.105783857G= NCBI36
NG_007069.1:g.56772C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.3746C= ENSP00000358748.3:p.Ala1249=
ENST00000647647.1:c.22C=
ENST00000648076.2:c.3992C= MANE Select ENSP00000497653.1:p.Ala1331=
ENST00000353479.9:c.3992C= ENSP00000340937.5:p.Ala1331=
ENST00000369733.7:c.3746C= ENSP00000358748.3:p.Ala1249=
NM_000494.3:c.3992C= NP_000485.3:p.Ala1331=
NM_000494.4:c.3992C= MANE Select NP_000485.3:p.Ala1331=