Canonical Allele Identifier: CA1933389678
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104037946T= , CM000672.2:g.104037946T= GRCh38
NC_000010.10:g.105797704T= , CM000672.1:g.105797704T= GRCh37
NC_000010.9:g.105787694T= NCBI36
NG_007069.1:g.52935A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.2936-173A= ENSP00000358748.3:n.2936-173A=
ENST00000648076.2:c.3071-173A= MANE Select ENSP00000497653.1:n.3071-173A=
ENST00000353479.9:c.3071-173A= ENSP00000340937.5:n.3071-173A=
ENST00000369733.7:c.2936-173A= ENSP00000358748.3:n.2936-173A=
NM_000494.3:c.3071-173A= NP_000485.3:n.3071-173A=
NM_000494.4:c.3071-173A= MANE Select NP_000485.3:n.3071-173A=