Canonical Allele Identifier: CA2576268176
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624572-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624572G>A , CM000679.2:g.41624572G>A GRCh38
NC_000017.10:g.39780824G>A , CM000679.1:g.39780824G>A GRCh37
NC_000017.9:g.37034350G>A NCBI36
NG_008625.1:g.5059C>T
NG_009090.2:g.167141C>T , LRG_401:g.167141C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-63C>T MANE Select ENSP00000308452.8:n.-63C>T
ENST00000311208.12:c.-63C>T ENSP00000308452.8:n.-63C>T
ENST00000463128.5:c.-313+171C>T ENSP00000468672.1:n.-313+171C>T
ENST00000491673.1:n.4C>T
NM_000422.2:c.-63C>T NP_000413.1:n.-63C>T
NM_000422.3:c.-63C>T MANE Select NP_000413.1:n.-63C>T
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