Canonical Allele Identifier: CA399512354
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624207C>A , CM000679.2:g.41624207C>A GRCh38
NC_000017.10:g.39780459C>A , CM000679.1:g.39780459C>A GRCh37
NC_000017.9:g.37033985C>A NCBI36
NG_008625.1:g.5424G>T
NG_009090.2:g.167506G>T , LRG_401:g.167506G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.303G>T MANE Select ENSP00000308452.8:p.Lys101Asn
ENST00000311208.12:c.303G>T ENSP00000308452.8:p.Lys101Asn
ENST00000463128.5:c.-312-1G>T ENSP00000468672.1:n.-312-1G>T
ENST00000491673.1:n.369G>T
ENST00000493253.5:n.90G>T
ENST00000540235.5:c.72-16G>T ENSP00000441751.2:n.72-16G>T
ENST00000577817.3:c.258G>T ENSP00000467418.1:p.Lys86Asn
NM_000422.2:c.303G>T NP_000413.1:p.Lys101Asn
NM_000422.3:c.303G>T MANE Select NP_000413.1:p.Lys101Asn