Canonical Allele Identifier: CA2637841056
Gene: KRT17 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624571T>C , CM000679.2:g.41624571T>C GRCh38
NC_000017.10:g.39780823T>C , CM000679.1:g.39780823T>C GRCh37
NC_000017.9:g.37034349T>C NCBI36
NG_008625.1:g.5060A>G
NG_009090.2:g.167142A>G , LRG_401:g.167142A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-62A>G MANE Select ENSP00000308452.8:n.-62A>G
ENST00000311208.12:c.-62A>G ENSP00000308452.8:n.-62A>G
ENST00000463128.5:c.-313+172A>G ENSP00000468672.1:n.-313+172A>G
ENST00000491673.1:n.5A>G
NM_000422.2:c.-62A>G NP_000413.1:n.-62A>G
NM_000422.3:c.-62A>G MANE Select NP_000413.1:n.-62A>G