Canonical Allele Identifier: CA2637840976
Gene: KRT17 HGNC NCBI

Linked Data

gnomAD v4: 17-41624548-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624548T>C , CM000679.2:g.41624548T>C GRCh38
NC_000017.10:g.39780800T>C , CM000679.1:g.39780800T>C GRCh37
NC_000017.9:g.37034326T>C NCBI36
NG_008625.1:g.5083A>G
NG_009090.2:g.167165A>G , LRG_401:g.167165A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-39A>G MANE Select ENSP00000308452.8:n.-39A>G
ENST00000311208.12:c.-39A>G ENSP00000308452.8:n.-39A>G
ENST00000463128.5:c.-313+195A>G ENSP00000468672.1:n.-313+195A>G
ENST00000491673.1:n.28A>G
NM_000422.2:c.-39A>G NP_000413.1:n.-39A>G
NM_000422.3:c.-39A>G MANE Select NP_000413.1:n.-39A>G
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