Canonical Allele Identifier: CA471502759
Gene: COL17A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.105793851G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104034093G>C , CM000672.2:g.104034093G>C GRCh38
NC_000010.10:g.105793851G>C , CM000672.1:g.105793851G>C GRCh37
NC_000010.9:g.105783841G>C NCBI36
NG_007069.1:g.56788C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369733.8:c.3762C>G ENSP00000358748.3:p.Pro1254=
ENST00000647647.1:c.38C>G
ENST00000648076.2:c.4008C>G MANE Select ENSP00000497653.1:p.Pro1336=
ENST00000353479.9:c.4008C>G ENSP00000340937.5:p.Pro1336=
ENST00000369733.7:c.3762C>G ENSP00000358748.3:p.Pro1254=
NM_000494.3:c.4008C>G NP_000485.3:p.Pro1336=
NM_000494.4:c.4008C>G MANE Select NP_000485.3:p.Pro1336=
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