Canonical Allele Identifier: CA1933420778
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104037696T= , CM000672.2:g.104037696T= GRCh38
NC_000010.10:g.105797454T= , CM000672.1:g.105797454T= GRCh37
NC_000010.9:g.105787444T= NCBI36
NG_007069.1:g.53185A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.3013A= ENSP00000358748.3:p.Ile1005=
ENST00000648076.2:c.3148A= MANE Select ENSP00000497653.1:p.Ile1050=
ENST00000353479.9:c.3148A= ENSP00000340937.5:p.Ile1050=
ENST00000369733.7:c.3013A= ENSP00000358748.3:p.Ile1005=
NM_000494.3:c.3148A= NP_000485.3:p.Ile1050=
NM_000494.4:c.3148A= MANE Select NP_000485.3:p.Ile1050=