Canonical Allele Identifier: CA399511779
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624122C>T , CM000679.2:g.41624122C>T GRCh38
NC_000017.10:g.39780374C>T , CM000679.1:g.39780374C>T GRCh37
NC_000017.9:g.37033900C>T NCBI36
NG_008625.1:g.5509G>A
NG_009090.2:g.167591G>A , LRG_401:g.167591G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.388G>A MANE Select ENSP00000308452.8:p.Asp130Asn
ENST00000311208.12:c.388G>A ENSP00000308452.8:p.Asp130Asn
ENST00000463128.5:c.-228G>A ENSP00000468672.1:n.-228G>A
ENST00000491673.1:n.454G>A
ENST00000493253.5:n.175G>A
ENST00000540235.5:c.139G>A ENSP00000441751.2:p.Asp47Asn
ENST00000577817.3:c.343G>A ENSP00000467418.1:p.Asp115Asn
NM_000422.2:c.388G>A NP_000413.1:p.Asp130Asn
NM_000422.3:c.388G>A MANE Select NP_000413.1:p.Asp130Asn