Canonical Allele Identifier: CA2789321285
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104037874dup , CM000672.2:g.104037874dup GRCh38
NC_000010.10:g.105797632dup , CM000672.1:g.105797632dup GRCh37
NC_000010.9:g.105787622dup NCBI36
NG_007069.1:g.53010dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.2936-98dup ENSP00000358748.3:n.2936-98dup
ENST00000648076.2:c.3071-98dup MANE Select ENSP00000497653.1:n.3071-98dup
ENST00000353479.9:c.3071-98dup ENSP00000340937.5:n.3071-98dup
ENST00000369733.7:c.2936-98dup ENSP00000358748.3:n.2936-98dup
NM_000494.3:c.3071-98dup NP_000485.3:n.3071-98dup
NM_000494.4:c.3071-98dup MANE Select NP_000485.3:n.3071-98dup