Canonical Allele Identifier: CA1933418115
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034098C= , CM000672.2:g.104034098C= GRCh38
NC_000010.10:g.105793856C= , CM000672.1:g.105793856C= GRCh37
NC_000010.9:g.105783846C= NCBI36
NG_007069.1:g.56783G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.3757G= ENSP00000358748.3:p.Gly1253=
ENST00000647647.1:c.33G=
ENST00000648076.2:c.4003G= MANE Select ENSP00000497653.1:p.Gly1335=
ENST00000353479.9:c.4003G= ENSP00000340937.5:p.Gly1335=
ENST00000369733.7:c.3757G= ENSP00000358748.3:p.Gly1253=
NM_000494.3:c.4003G= NP_000485.3:p.Gly1335=
NM_000494.4:c.4003G= MANE Select NP_000485.3:p.Gly1335=