Canonical Allele Identifier: CA1933420732
Gene: COL17A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104037599G= , CM000672.2:g.104037599G= GRCh38
NC_000010.10:g.105797357G= , CM000672.1:g.105797357G= GRCh37
NC_000010.9:g.105787347G= NCBI36
NG_007069.1:g.53282C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369733.8:c.3073+37C= ENSP00000358748.3:n.3073+37C=
ENST00000648076.2:c.3208+37C= MANE Select ENSP00000497653.1:n.3208+37C=
ENST00000353479.9:c.3208+37C= ENSP00000340937.5:n.3208+37C=
ENST00000369733.7:c.3073+37C= ENSP00000358748.3:n.3073+37C=
NM_000494.3:c.3208+37C= NP_000485.3:n.3208+37C=
NM_000494.4:c.3208+37C= MANE Select NP_000485.3:n.3208+37C=